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Head of Enforcements Location: Liverpool Salary: £Competitive Contract Type: Perm Position Type: Full Time Bond Turner is a leading law firm, proudly recognised by both Legal 500 and Chambers & Partners. We are committed to ensuring access to justice for our clients and their families, providing expert legal services with a client-centered approach. With offices in Liverpool and Bolton, we offer nationwide legal advice across a wide range of sectors. Our areas of expertise include Credit Hire, Personal Injury, including Complex Injury, Clinical and Professional Negligence, Housing Disrepair, Group Action Claims and Public Inquiries. We are driven by a commitment to achieving successful outcomes, surpassing client expectations, and creating a supportive environment that empowers our employees to build fulfilling and rewarding careers. We understand that our growth as a business is driven by the success of our people. We take pride in fostering a positive, collaborative work environment where everyone can contribute to our shared success. With exceptional support at every turn, every employee is empowered to reach their full potential. The Head of Enforcement leads the firm’s enforcement and recovery function, overseeing the execution of court judgments, debt recovery strategies, asset tracing, and enforcement proceedings. This role ensures efficient, compliant, and commercial enforcement activities while driving client satisfaction and revenue generation. Key Responsibilities Leadership & Strategy • Develop and implement the firm’s enforcement strategy aligned with business objectives, • Lead, manage, and mentor the enforcement team (lawyers, paralegals, support staff), • Monitor performance targets (recoveries, timelines, cost efficiency) and monitor delivery, • Drive innovation in enforcement processes, including use of technology and data Enforcement & Recovery Management • Oversee all enforcement actions, including:, • Part 8 procedures’, • Writs/warrants of control, • Charging orders, • Attachment of earnings orders, • Third-party debt orders, • Insolvency actions (bankruptcy/winding-up), • Advise on complex or high-value enforcement strategies, • Supervise asset tracing and recovery efforts, • Ensure effective case progression from judgment to recovery, • Ensure all enforcement activities comply with relevant legal and regulatory frameworks (e.g., FCA, SRA, CPR), • Oversee complaints handling related to enforcement actions Client Relationship Management • Act as senior point of contact for clients, • Provide strategic advice on enforcement options and risks, • Deliver regular reporting on recovery performance and outcomes Operational Performance • Improve workflow efficiency and case management systems, • Track KPIs including recovery rates, turnaround times, and client satisfaction Key Skills & Experience Essential • Qualified solicitor (or equivalent) with significant experience in litigation and enforcement, • Strong technical expertise in civil procedure rules and enforcement mechanisms, • Proven leadership and team management experience, • Commercial awareness and client-focused mindset, • Experience handling high-volume and high-value enforcement portfolios Desirable • Previous experience with Proclaim, • Experience in debt recovery, insolvency, or asset recovery, • Familiarity with enforcement technology platforms and data analytics, • Established client relationships or business development track record Key Competencies • Strategic thinking and alignment, • Leadership and people development, • Negotiation and influencing skills, • Attention to detail and risk awareness, • Results-driven with strong accountability Reporting Line • Reports to: Director/ Head of Litigation, • Direct reports: Enforcement team (lawyers, paralegals, admin) Company Values: We’re a collaboration of companies established in 2006 working towards and guaranteeing the same goal. Our mission: We are driven to succeed. Our purpose is to help people move on in their lives through supporting our clients, our communities and each other. • We support, • We surpass, • We succeed What we offer in return: We offer a clean professional office working environment with fantastic facilities in the heart of Liverpool City Centre which has great travel links. • A competitive salary, • 23 days holiday + your Birthday off + plus 8 bank holidays., • Income protection, dental plan, critical illness cover & death in service cover, • Employee Assistant Programme., • Workplace pension scheme., • Free onsite weekly classes and well-being programmes., • Discounted onsite Restaurant, Coffee Shop / Café., • Secure bike storage., • The opportunity to develop a rewarding and successful career with a wonderful Law firm.

Unlock Your Future in Life Sciences Programming at Quanticate! Are you a skilled SAS Programmer with a strong grasp of SQL? Ready to leverage your technical expertise in impactful Real World Evidence (RWE) life science projects rather than finance or other industries? Join Quanticate, one of the world's leading data-focused CROs, where you’ll contribute to some of the most advanced clinical programs across the globe. Be a part of projects that contribute to the advancement of therapies that genuinely make a difference in patients' lives. Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotech’s that are taking their first steps in clinical development We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter. This is a fully remote role but candidates must be based in UK or Poland due to employment contracts. Procedures: • Program tables, figures and listings and derived datasets according to the request description., • Perform quality control checks and complete quality control documentation for programming plans, specifications, outputs/derived datasets., • Perform other reasonable programming tasks as requested by management., • Follow appropriate Project Management procedures., • Communicate effectively with OR team., • Provide input to improvements to processes, procedures and standards., • Support the training and development of other programmers. Objectives: • Further development of knowledge of SAS and advanced SQL, good programming practices and numerous Real World Data (RWD) databases., • Ensure high levels of customer care are provided., • Review available resources to find required information, • Use and manipulate data stored in SQL database., • Ability to understand and modify SAS macros., • Use longitudinal databases (Administrative medical and pharmacy claims databases, Electronic Medical Records)., • Technical experience in handling large datasets., • Basic understanding of statistical models used in Outcomes Research (OR), • Ability to ask questions effectively., • Extensive knowledge of statistical software packages (particularly SAS),, • Extensive knowledge of SQL, • Qualified to degree level or equivalent, preferably in a numerate discipline., • Experience with large datasets, ideally, Medical data - Healthcare databases, Payer databases, Hospital records, • Should have PC skills, • Good organisational skills, communication skills (oral and written), • Good analytical skills and attention to detail., • Private medical care, • Life insurance, • Flexible working time, • Full time home working

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on . Senior Statistical Programmer Job Specific Skills: • Mastery and trained on generating tables, listings, and graphs from clinical trial databases using SAS., • Utilizes System Development Life Cycle (SDLC) for programming deliverables., • Advanced user in SAS programming, SAS Base, and SAS Macros., • Advanced knowledge of E-Submission Standards, Guidelines and Regulations., • Mastery and trained on SDTM standards including ability to write specifications., • Advanced knowledge of ADaM standards including supporting specification writing., • Proficient with MS Office applications., • Advanced knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirements., • Advanced experience with pooling of data sets for submissions., • Advanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP., • Lead study or small programming project teams. Job Requirements: • Masters required for all Statistics roles., • Minimum of 5 years’ experience in Statistical Programming or similar field required., • Expert knowledge of scientific principles and concepts., • Reputation as emerging leader in field with sustained performance and accomplishment., • Proficiency with MS Office applications., • Hands-on experience with clinical trial and pharmaceutical development preferred., • Good communication skills and willingness to work with others to clearly understand needs and solve problems., • Excellent problem-solving skills., • Good organizational and communication skills., • Familiarity with current ISO 9001 and ISO 27001 standards preferred., • Familiarity with 21 CFR Part 11, FDA, and GCP requirements., • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process. Should you not have received a response within 14 days of your application, please consider your application unsuccessful.

The Role uMotif’s Customer Support team is looking for a UK based Support Specialist who would be responsible for supporting customers during core UK business hours. The role is based remotely in the UK, although the current team is based in both the UK and US and covers the UK, European and US time zones. In this role, you will provide day to day technical and customer support for our data capture solutions. This includes being responsible for and triaging support tickets as they are received which can vary from assisting our users, making database data changes, producing data reports and extracts, investigating and solving technical issues and supporting your team and the wider business to provide an exceptional support service. At the core of the role is the ability to interrogate, manage and update captured data using SQL/MYSQL whilst adhering to data privacy and regulated data management guidelines, so we ask for 3+ years of experience providing customer support with at least 2 years demonstrable SQL skills. What will you do? • Serve as the escalation point for support cases including overall triage., • Help maintain and support our internal ticketing tools and communication channels., • Investigate and resolve 1st, 2nd and some 3rd line support issues., • Escalate complex 3rd line support issues if unable to resolve within the team., • Ensure issues are responded to within predefined company SLAs., • As a team provide continuous product support during core UK, Europe and US working hours., • Work with our third party 1st line support vendor ensuring a seamless support service., • Provide support to system users in multiple countries predominantly via email and our support ticketing system, with occasional client calls as needed., • Build professional rapport with internal and external clients by demonstrating empathy and strong communication skills and clearly document all communication with system users., • Follow up with customers to ensure full resolution, providing timely updates of progress along the way., • Become proficient in core applications in the uMotif product suite and share this knowledge with all other internal cross-functional teams as necessary., • Work in harmony with all business departments to ensure a complete support function., • Promote good practice and contribute towards knowledge sharing and process documentation., • Develop an understanding of customer processes and standard operating procedures., • Gain knowledge of clinical research workflows to support understanding and context of customer questions., • Facilitate troubleshooting and communication across multiple teams to provide customers with effective solutions quickly. When a solution is not readily available, collaborate with other internal resources., • Demonstrate responsiveness and sense of urgency in all customer interactions., • Advocate for customers by tracking and communicating suggestions for software enhancements., • Perform other job-related duties as assigned. What you need to succeed • Prior technical support experience is preferred, especially in healthcare, life sciences, clinical research or related fields., • 3+ years of experience providing customer support with at least 2 years demonstrable SQL skills., • Excellent verbal and written communication skills and the ability to work optimally in a remote team environment., • Initiative and desire to learn new skills/technologies and remain up-to-date with the latest trends., • Excited by firefighting and a real passion for solving technical problems., • Experience working with and improving support ticketing systems, ideally Jira Service Management., • Committed to working within a team that promotes the uMotif culture., • Thrives in a fast-paced, dynamic environment., • A team player who puts the success of the team first and is motivated by helping clients and finds satisfaction in helping to resolve the issues of others., • A resourceful problem-solver who seeks out effective and efficient solutions., • Strong time management skills and ability to effectively manage multiple priorities., • Experience working within regulated environments, for example GDPR, GCP & HIPAA., • Any exposure to the following would be a real bonus: Command Line, PHP, Python, CSS, HTML, XML, JSON, Javascript., • Any experience with the following tools: Jira, AWS, Jira Service Management, Tableau, Slack, Gitlab, iOS & Android environments, MDM, Microsoft Office & GSuite. Why uMotif? • Unlimited paid holiday allowance after probation, • Contributory Salary Sacrifice pension, • Private Health Insurance via Vitality, • Simplyhealth cashback scheme, • 5x salary Life Insurance, • Full pay for the first 13 weeks of SMP during maternity leave, • Perkbox subscription, • Salary Sacrifice Cycle scheme, • Remote working, • Home office allowance, • WFH expense contribution About us Our Company uMotif’s mission is to put patients at the centre of research by building data capture solutions people love to use. Designed with patients for patients, the uMotif platform supports data capture for each phase of clinical research across all therapeutic areas. Over 22,000 participants use our applications to track and submit e-consent, symptom, eCOA, ePRO, and wearable device data. With expertise in engaging patients and fast deployments, we work with ten of the top twenty global pharmaceutical companies to power large real-world evidence (RWE) and virtual studies. Our core values: Patients First - We care about patients and put them first; from our products to our business decisions. Teamwork - Through collaborating with and supporting each other, our customers, and our partners we succeed together. Innovation - We work innovatively to design, build, and deliver engaging technology. Team uMotif are united in our belief that patient-centric thinking combined with beautiful technology and effective teamwork can truly change clinical research for the better. We search for mission-driven people who are not afraid to be challenged - who want to tackle demanding problems and embrace innovative ideas. uMotif is an equal opportunities employer We positively encourage applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity. We want everyone at uMotif to be comfortable bringing their true self to work. That means acknowledging your personality, including the quirky bits, and bringing your interests, hopes, dreams, and even fears with you is fine, even if they don't seem relevant to your work.

Company OverviewEmbark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. At PROCEPT, we put the patient first in everything we do and are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders. That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities. Reporting to the Sales Director, UK & Ireland, the Senior Account Manager, UK will be responsible for achieving sales revenue targets by developing, implementing and overseeing the execution of strategic plans with hospital targets, teaching institutions and key private groups in the assigned geography. The major responsibilities are to manage and direct the utilization of Aquablation Therapy within their installed base. This will include managing installations, training and utilization growth within their assigned region and the hiring, training, and development of Aquablation Clinical Sales Representatives and Associate level roles. • Meet or exceed quarterly sales quota for the defined area and target hospitals, • Work with the sales manager to develop a territory plan that outlines sales objectives tailored to the local market, • Manage and develop identified key opinion leaders within territory, • Provide quarterly updates on the territory and account performance, • Lead Aquablation Programme Reviews and follow Surgical Pathway for all Aquablation surgeons, • Lead local marketing activities and develop joint marketing plan with accounts to increase patient awareness, • Provide weekly/monthly forecasts for defined area, • Direct and support team members within the defined area to over achieve goals and quotas, • Support the internal development & training of associate and junior team members, • Effectively communicate Aquablation’s value proposition to customers, • Work with senior hospital staff and key surgeons in the development and execution of a plan to effectively integrate the Aquabeam system at new customer sites and ensuring ongoing commitment to the system, • Develop an Aquablation plan for each surgical team to support independent use of the technology, • Drive utilization of the Aquabeam System by collaborating with surgical teams to support usage of the technology, • Drive continuous expansion of the user base by working with key hospital staff and thought leaders to develop a qualified lead funnel. Regular activities consist of formal presentations, informal events, and get-togethers, • Effectively convert high potential leads and drive training activities, • Drive sales through new product introductions and solution selling, • Qualify, train, assess, and ultimately develop accounts to adopt the AquaBeam’s system as an integral part of their BPH practice with the goal of demonstrating high account adoption, • Partner with the Professional Education team to deliver outstanding clinical and training support to physicians so that physicians can quickly become clinically independent, • Build and maintain relationships with key customers and KOLs within region, • Partner closely with Sales Management and the Marketing team to identify and prioritize customers for higher-level corporate relationships, • Partner with the Customer Service team to meet and exceed customer expectations, • Ensure all required sales reporting forms are completed and submitted on time, • Maintain records in the PROCEPT CRM system on contacts and facilities, • Provide support in the resolution of product complaints and/or safety issues, • Proactively support organizational goals and objectives, policies and procedures, and FDA regulations including strict compliance with AquaBeam’s Customer Relationship and the Sunshine Act policies, • Maintain a professional and credible image with customers and teammates, • Establish and maintain credentials to enter and work in hospitals and other medical facilities as required by facility requirements, • Manage travel and expenses per approved budget, • Maintain trained status for, and comply with, all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance, • Understand and adhere to the PROCEPT BioRobotics Quality & EHS policies, • Bachelor’s degree from accredited reputable institution, • A minimum of 8 years of experience in medical sales within the Urology space or Operating Room, and 8 years of total sales experience, • Start-up company experience selling disruptive surgical technology, • Experience introducing market development programs to physician practices, • Strong local relationships within the healthcare community in specified geographic area, • Leadership skills as demonstrated through past professional performance, involvement in sports, professional clubs, or associations, • Ability to travel upwards to 75%Understanding PROCEPT's CultureAt PROCEPT, we believe every person matters. Every employee, every patient, every caregiver. Because we are here to create a revolution, and we believe in doing that by innovating everywhere with pathological optimism. We believe in being humble and highly engaged in the work we do, while also working together seamlessly for a common goal. At Procept, curiosity, ingenuity and conviction in the power technology will transform the lives of our patients and providers. And this doesn’t happen by accident. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept’s history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do. It continues with our one-of-a-kind management program designed to build the best managers in the industry, where our people managers across functions come together to exchange ideas and grow, as both managers and learners, in an environment that challenges, supports and broadens. We are fueled by the opportunity to give people their lives back. And we believe that it begins with YOU! At Procept, we push beyond just finding a work/life balance, we strive to find a work/life blend, a professional world that you are honored and impassioned to belong to, one that you can proudly share with your family, friends, and acquaintances. An opportunity at PROCEPT BioRobotics won’t just be about finding a job. It will be an opportunity for you to join a community devoted to making a difference in this world! BENEFITS OF WORKING AT PROCEPT! PROCEPT’s health and wellness benefits for employees are second to none in the industry. As an organization, one of our top priorities is to maintain the health and wellbeing of our employees and their families. We offer a comprehensive benefits package that includes full medical coverage, wellness programs, on-site gym, a 401(k) plan with employer match, short-term and long-term disability coverage, basic life insurance, wellbeing benefits, flexible or paid time off, paid parental leave, paid holidays, and many more! EQUAL EMPLOYMENT OPPORTUNITY STATEMENTPROCEPT BioRobotics is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind on the basis of race, color, national origin, religion, gender, gender identity, sexual orientation, disability, genetic information, pregnancy, age, or any other protected status set forth in federal, state, or local laws. This policy applies to all employment practices within our organization. PAY RANGE TRANSPARENCYProcept is committed to fair and equitable compensation practices. The pay range(s) for this role represents a base salary range for non-commissionable roles or on-target earnings for commissionable roles. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, relevant certifications and training, and specific work location. Based on the factors above, Procept utilizes the full width of the range. The total compensation package for this position may also include eligibility for annual performance bonus, equity, and the benefits listed above. WORK ENVIRONMENTWe’ll provide you training for, and ask you to maintain trained status for, and comply with, all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance. We would also ask you to understand and adhere to the PROCEPT BioRobotics Quality & EHS policies. PROCEPT BioRobotics – Applicant Privacy NoticeWhen you submit an application on this site, PROCEPT BioRobotics collects the personal information you provide. This may include your name, email address, phone number, résumé or CV, LinkedIn profile, and any optional demographic information you choose to share, such as gender or ethnicity. We use this information to review your application and assess your suitability for the role. To learn more about how we handle personal information, including your rights under applicable privacy regulations, please read our full Privacy Notice at: [_].We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients in CVRM team. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. Main Job Tasks and Responsibilities: The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Requirement: • Strong SAS programming experience within the pharmaceutical/CRO industry, • Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies, • Experience in generating and validating SDTM, ADaM, and TLFs, • Good understanding of CDISC standards and clinical trial processes, • Ability to work independently and manage multiple priorities in a fast-paced environment, • Experience supporting regulatory submissions is preferred, • Strong communication and stakeholder management skills Responsibilities: • Develop, validate, and maintain SAS programs for clinical study data analysis and reporting, • Create datasets, tables, listings, and figures according to study requirements, • Collaborate with Biostatistics, Data Management, and Clinical teams, • Ensure programming deliverables meet quality standards and project timelines, • Participate in study planning, review specifications, and support submission activities Education and Experience: • Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience., • Need to have Respiratory/Immunology TA experience., • Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. #LI-TT1 #LI-Remote #Senior #Contract

May manage department Clinical Project Managers, Assistant Project Managers, Clinical Trial Associates and other supporting staff. Ora's pre-clinical and clinical models, unique methodologies, integrated clinical data solutions, and global regulatory strategies have been refined and proven across th

🕙 Role details: This is a full time role for 40 contracted hours per week 💷 Salary: £75,000 – £95,000 per annum + Uncapped commission + equity options 🌍 Location: We are a hybrid team, based throughout the UK. We offer the flexibility to work outside of the UK up to 90 days per year, however you must be able to work and live permanently within the UK, and travel to London at least 4 times a year for team meeting sessions and additionally as needed. #LI-Remote ------ We’re looking for a talented Partnership Lead to join Isla’s Sales team. In this dynamic role, you’ll lead complex sales cycles and high-level, vision-led pitches to NHS executive stakeholders (COOs, CDIOs, and CFOs). As a senior hire, you will materially improve our ability to hit revenue targets by owning high-value NHS opportunities end-to-end. The ideal candidate will bring "insider" NHS knowledge and a sense of seniority that gives stakeholders immediate assurance. While harnessing relationship building, you will also rely on credibility and quantitative skills to build robust financial opportunity models and compelling business cases that quantify the impact of Isla deployments. ------ Isla Health is a venture-backed healthtech startup, supporting our partners across the UK, EU and internationally beyond this. We have built a new category of healthcare technology which we refer to as the Digital Pathway Platform (DPP). Founded in 2019, we now support 25% of NHS Trusts and a submission of patient data is made on the platform every 20 seconds. As a company we are all laser focused on enabling a scalable model of care which empowers healthcare staff and improves patient outcomes. The DPP supports this by setting up digital pathways which are remote-first and asynchronous. As pathways harness sophisticated automation, clinical algorithms and intelligent cohorting, patients always take the optimised route through their pathway, thereby delivering a step change in clinical productivity. ------ • Own the executive pitch: Lead vision-led conversations with NHS C-suite stakeholders, focusing on system-wide impact rather than just product features., • Lead executive-level engagement: Own a portfolio of strategic opportunities, navigating NHS governance and procurement to move deals from identification to close., • Develop quantitative business cases: Use Google Sheets/Excel to build robust financial models that translate messy operational reality into structured numbers for execs., • Leverage your network: Use your existing NHS connections and "insider" status to open doors and navigate complex procurement and governance routes., • Drive strategic growth & shape commercial strategy: Feed structured market insights back into the business to steer key decisions and the product roadmap., • Collaborate cross-functionally: Work with our Product and Delivery teams to ensure the commercial promises we make align with clinical reality., • NHS "Insider" credibility: You have either sold heavily into the NHS at scale (enterprise deals) or you have worked within the NHS in a senior capacity. You "speak the language" and understand how decisions actually get made., • Quantitative & data rigour: You are highly comfortable in Google Sheets/Excel. You can build your own financial models and business cases to prove ROI to NHS Finance Directors., • Executive credibility: You have experience pitching to or working directly with NHS executives (COOs, Medical Directors, etc.) and command natural seniority and confidence., • Strategic thinking: The ability to navigate long sales cycles and position Isla within national and regional priorities., • Enterprise sales track record: Success in leading large, consultative deals or transformation programmes within healthcare., • Passion & energy: A deep desire to solve global problems and make a positive change in patient healthcare. Benefits 🏡 Work from home or at our office in 131 Finsbury Pavement - Industrious 🏢 📈 Equity options and 5% pension contributions. 🕜 Flexible working times 🌍 Work abroad for up to 90 days per year 🎉 Enhanced parental leave 🏖️ 25 days annual leave (on top of bank holidays) 🎂 Take your birthday off 🎄 Take Christmas Eve off too 🍜 Treat your friends or family to a meal each quarter (up to £75) 🧘‍♀️ A monthly wellbeing bonus (£50 per month for gym membership/wellbeing activities) or Private medical 🎳 Bi-monthly team socials and a meal out 📚 A learning budget for you to use 💗 Delivering social impact through improved patient healthcare 💡 Working at a well funded and rapidly growing start up, solving a global problem in a new way 🎇 A whole lot of fun on an exciting journey ------ What is the hiring process for this role at Isla? 1️ A screening interview with our Associate Operations Manager - 20 minutes 1. Take-home written task, 2. A one-to-one pitch interview with our Director of Partnerships - 45 minutes, 3. A final interview with our Director of Partnerships and one of our Co-founders - 30 minutes ------ Diversity and Inclusion Isla is an equal opportunity employer and is committed to building an inclusive and diverse team. We encourage all qualified candidates to apply. Isla does not discriminate against anyone on the basis of their race, gender, disability, religion, national origin, age, or any other protected category. We choose to celebrate our team’s differences and see them as one of our most valuable assets. Recruitment is not one-size-fits-all and we're happy to tailor our hiring process to better meet the needs of individual applicants. Please email recruitment@isla.health with any requests for support.

Job Purpose As a Specialist IT, you will report to the Head of IT and serve as a key technical person for our Cambridge site, while providing essential support in managing our IT infrastructure and ensuring the smooth operation of our Microsoft 365 ecosystem in collaboration with the rest of the Team. Your role will encompass a diverse range of responsibilities, making this an exciting and dynamic opportunity for IT professionals who thrive in a collaborative and evolving environment. You will have a some focus on our ERP systems such as Veeva and/or SAP. Your profile Major Accountabilities: Microsoft Expertise: Leverage your strong knowledge of Microsoft Azure and Microsoft 365 tools, including but not limited to Intune, Autopilot, Defender, SharePoint, Teams, to optimize and secure our IT environment. Veeva & ERP Support: User and systems support for our Veeva and SAP products. Collaborate with business stakeholders to ensure these systems align with operational needs and compliance standards IT Support: Provide top-notch technical support to our employees both remote or onsite, troubleshooting issues and ensuring smooth IT experience for all. Deliver training to enhance adoption and efficiency. Assist with onboarding and offboarding of users and devices, ensuring smooth transitions and access control. Infrastructure Management: Assist in the management, implementation and maintenance of our IT infrastructure, including servers, networks and cloud-based systems. Security and Compliance: You will have a very strong security mindset and will collaborate to implement and monitor with security measures to protect our sensitive data and ensure compliance with industry standards. Collaboration: Facilitate collaboration among teams by proposing new solutions and optimizing tools like Microsoft Teams, SharePoint, Zoom, etc. Project Participation: Contribute with your expertise to IT projects aimed at enhancing our technology capabilities and efficiency. Document technical solutions and contribute to the IT knowledge base to support continuous improvement and team learning. Adaptability: In the early stages of our IT department’s growth, be prepared to wear multiple hats and assist with various IT-related tasks and challenges as needed. Job Requirements: • Education: Bachelor’s degree in Information Technology, Computer Science or a related field or proven experience., • Good knowledge of Veeva products or SAP products is a plus., • Strong proficiency in Microsoft 365 tools and services., • Proven experience in IT system administration and support., • Excellent problem-solving and communication skills., • Ability to work collaboratively in a fast-paced, dynamic environment. Work Location: • 2 to 3 days a week in our brand new Cambridge Office. Why us? An exciting job opportunity awaits you! MoonLake is a dynamic and innovative company pushing the boundaries of possibility, and we are looking for passionate individuals to join our stellar team. What we offer: Learning Environment: An opportunity to learn and grow alongside experienced professionals in a supportive and innovative biotech environment. Impactful Work: Contribute to groundbreaking projects that have the potential to transform global healthcare. Flexibility and Balance: Work remotely/hybrid, enjoying a healthy work-life balance while making meaningful contributions to our team. Career Growth: A clear path for career progression, with the chance to take on more responsibilities as you develop your skills. About us MoonLake Immunotherapeutics is a clinical-stage biopharmaceutical company unlocking the potential of sonelokimab, a novel investigational Nanobody® for the treatment of the inflammatory disease, to revolutionize outcomes for patients. We continue to make significant progress in our Global Clinical Development Programs. The company’s focus is on inflammatory diseases with a major unmet need, including hidradenitis suppurativa and psoriatic arthritis – conditions affecting millions of people worldwide with a large need for improved treatment options. MoonLake was founded in 2021 and is headquarted in Zug, with hubs in Cambridge & Porto. Further information is available at _

About DPBIO DPBIO is a pioneering innovator based in California, specializing in high-throughput droplet microfluidic technology and providing cutting-edge life science solutions to researchers and industry leaders worldwide. At DPBIO, we integrate advanced microfluidic technology with life sciences to develop comprehensive solutions, including microfluidic chips, instruments, and reagents. Our flagship products—such as the CytoSpark® High-throughput Screening System, OMNIdrop System—empower scientists in antibody discovery, enzyme evolution, strain screening, small-molecule drug screening, cancer research, early disease detection, viral quantification, and biopharmaceutical quality control. Trusted by leading biotech and pharmaceutical companies, top-tier research institutions, and clinical laboratories worldwide, DPBIO is committed to advancing life sciences with high-performance analytical and detection systems. Our mission is to accelerate drug discovery, synthetic biology, biomedical research, and precision medicine, driving breakthroughs that transform life science innovation. We are seeking a highly driven Business Development Manager to lead market expansion for DPBIO’s antibody discovery platform across the Europe and UK This role will be responsible for developing strategic partnerships, driving revenue growth, and expanding DPBIO’s presence within biotech, pharmaceutical, and antibody discovery ecosystems in the western territory. Essential Duties · Sales Management: Develop and execute sales strategies to achieve revenue targets. Identify and pursue new business opportunities while nurturing existing client relationships. · Client Support: Oversee and manage all aspects of customer support to ensure high levels of satisfaction and prompt resolution of issues. Act as the primary point of contact for key accounts. · Market Insights: Monitor and analyze market trends, competitor activities, and customer feedback. Use insights to inform sales strategies and improve service offerings. · Customer Engagement: Build and maintain strong relationships with clients and stakeholders. Conduct regular meetings and reviews to understand their needs and provide tailored solutions. · Sales Reporting: Prepare and present regular reports on sales performance, support metrics, and market developments to senior management. Utilize data to drive decision-making and strategic planning. · Process Improvement: Identify and implement improvements to sales processes and support procedures to enhance efficiency and effectiveness. · Business Development: Identify and pursue new business opportunities, partnerships, and markets within East Coast of the United States to drive revenue growth and expand market share. · Strategic Planning: Develop and implement regional strategies aligned with DPBio’s overall business objectives, ensuring effective market penetration and competitive positioning. · Client Relationship Management: Build and maintain strong relationships with key clients, partners, and stakeholders. Provide exceptional service and support to ensure customer satisfaction and loyalty. Territory & Commercial Ownership： Lead market expansion for DPBIO’s antibody discovery platform across Europe and UK Extensive experience in the full sales cycle, from lead generation and technical consultation through negotiation and successful deal closure Documented track record of closing complex, high-value scientific or platform-based deals Antibody Domain Expertise (Required)：5+ years of experience in the antibody discovery or biologics development field Cell Sorting & Single-Cell Knowledge Flow cytometry and FACS platforms Established relationships within Antibody-focused biotech companies， Immunology research groups， Biologics discovery teams

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. Main Job Tasks and Responsibilities: The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Responsibilities: • Responsible for supporting the Programming deliveries of a clinical study or project., • Implements statistical programming aspects of the protocol and the clinical development program., • Ensures high quality is built into own deliverables and the quality delivered by other programmers., • Programs independently with high efficiency and quality., • Writes and/or implements specifications and oversees completeness of relevant documentation., • Contribute to the development of best practices to improve quality, efficiency, and effectiveness within the function., • Ensures compliance with standards and automation usage., • Plans and support team activities and tasks., • Communicates and escalates risks within the assigned studies and/or projects., • Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader. Education and Experience: • Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience., • Need to have Oncology TA experience., • Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology., • Good understanding of the clinical drug development process., • Strong communication skills and coordination skills., • Current knowledge of technical and regulatory requirements relevant for the role, • Ability to proactively manage concurrent activities within a project, • Proficient ability to influence relevant stakeholders on programming-related items The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. #LI-DNP

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. Main Job Tasks and Responsibilities: The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Responsibilities: • Responsible for supporting the Programming deliveries of a clinical study or project., • Implements statistical programming aspects of the protocol and the clinical development program., • Ensures high quality is built into own deliverables and the quality delivered by other programmers., • Programs independently with high efficiency and quality., • Writes and/or implements specifications and oversees completeness of relevant documentation., • Contribute to the development of best practices to improve quality, efficiency, and effectiveness within the function., • Ensures compliance with standards and automation usage., • Plans and support team activities and tasks., • Communicates and escalates risks within the assigned studies and/or projects., • Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader. Education and Experience: • Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience., • Need to have Oncology TA experience., • Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology., • Good understanding of the clinical drug development process., • Strong communication skills and coordination skills., • Current knowledge of technical and regulatory requirements relevant for the role, • Ability to proactively manage concurrent activities within a project, • Proficient ability to influence relevant stakeholders on programming-related items The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. #LI-TT1 #LI-Remote #Senior #Contract

Measure, track, and report on product KPIs to internal and external stakeholders, providing data-driven rationale for product pivots and investments. Work closely with Legal and Clinical teams to ensure all product features comply with UK-specific data residency requirements, GDPR, and international

The role is remote for people based in the UK What is the job? We are looking for a hands-on, delivery-focused Business Change Specialist to help turn improvement ideas into real, operational change. This role is about making things happen - quickly - in a fast-growing, highly regulated health-tech environment. You will work across the business to implement projects big and small, with a strong focus on improving the end-to-end patient journey. From mapping processes and fixing friction points to embedding new ways of working, you’ll be on the ground driving change, not just designing it. You’ll partner closely with teams throughout the business and a Project Manager on larger initiatives, while owning and delivering your own portfolio of improvements. You will need to be comfortable with pace, ambiguity, and getting stuck in wherever the biggest impact sits. This is an ideal role for someone with strong Lean and customer-journey experience who is pragmatic, scrappy, and biased to action - someone who thrives in a start-up environment and takes real satisfaction from shipping improvements that stick and make life better for patients and teams alike. What will you be doing? Deliver improvement initiatives end-to-end, from problem definition through to implementation and measurable outcomes. Work across the business to lead and support hands-on implementation of changes, ensuring solutions are practical, adopted by teams, and embedded into day-to-day operations. Map, analyse, and improve end-to-end patient journeys, identifying sludge and friction, process defects, and root causes. Apply Lean Six Sigma tools to diagnose issues, design countermeasures, and drive rapid, iterative improvement. Own discrete projects and workstreams, while supporting the wider business on larger programmes as required. Translate insights into clear process documentation (process maps, SOPs, work instructions, controls). Facilitate workshops to align stakeholders on current state, future state, and implementation actions. Coordinate delivery across cross-functional teams, keeping momentum in a fast-paced, changing environment. Track and report on outcomes to ensure changes improve patient experience, efficiency, and quality. Identify risks, blockers, and dependencies early and escalate pragmatically, whilst remaining solution-oriented. Drive standardisation and right-first-time ways of working across operational teams. Use data, customer feedback, and complaints insights to prioritise and shape improvements. Support change adoption through training, communication, and ongoing feedback loops. Act as a versatile problem-solver, able to get stuck into any type of business improvement as priorities shift. Operate with an agile, “get things done” start-up mindset, adapting quickly and prioritising delivery over perfection. Define success measures of initiatives at the outset and use these to validate success/control once delivered. Ensure all changes are compliant with relevant clinical/pharmaceutical regulation and other internal governance requirements. What do you need? Proven experience implementing operational or customer journey improvements in a fast-paced highly-regulated environments. Demonstrable ability to move quickly from analysis to action and deliver tangible change. Solid stakeholder management and facilitation skills across cross-functional teams. Experience supporting project delivery or working within structured and semi-structured project environments. Willingness to travel to Winnersh to meet stakeholders from time to time What we offer: Competitive salary 25 days holiday (rising to 27 after one year and 30 after two years) + bank holidays 5% matched pension Cycle-to-work scheme Enhanced Maternity & Paternity Leave Opportunities for development and growth A dynamic and supportive work environment About Montu Montu UK is a leading digital health company specialising in cannabis-based medicines (CBPM). We are committed to transforming lives by improving access to safe, effective treatments and offering an exceptional standard of care. Our dynamic and supportive work environment is the perfect place for you to grow professionally while making a meaningful impact on patients’ lives.

New Hospitals Programme Salary - £600 per day outside of IR35 Contract / Associate flexible engagement The Opportunity Our NHS client are progressing major schemes under the New Hospitals Programme (NHP). As we move from concept into delivery, were looking for an experienced digital professional to shape how future hospitals are digitally enabled from the ground up. This role sits at the intersection of digital, estates, clinical operations and hospital design. Its about helping teams think differently and practically about how technology, data and smart infrastructure can transform care delivery in new hospital buildings. What Youll Be Doing • Leading and facilitating conversations with clinicians, operational teams, estates and digital colleaguesabout whats now possible in a digitally-enabled hospital, • Translating Hospital 2.0 / NHP blueprintsinto real, usable digital capabilities within building designs, • Shaping approaches to:, • Smart buildings & sensor-enabled infrastructure, • Digital twins, • Integrated command, control and data platforms, • Digitally-enabled clinical workflows, • Bridging the gap between design intent and operational reality, • Producing clear, pragmatic outputsthat inform design, investment and delivery decisions (not slide-ware for its own sake) What Were Looking For • Strong digital background(healthcare preferred, but not essential if youve worked on complex, tech-enabled new builds), • Experience with large-scale new-build or major infrastructure programmes, ideally involving innovative technology, • Comfortable leading workshops and discussions with senior clinicians and operational leaders, • Able to thought-lead when required but listen deeplyand co-design solutions, • Practical, delivery-focused, and credible nottraditional management consultancy Must Have • NHS or healthcare system experience, • Exposure to NHP, Hospital 2.0 thinking, or major public sector capital programmes, • Experience of embedding digital thinking early into estates and engineering decisions Engagement & Commercials • Contract / associate basis, • Funded through the New Hospitals Programme, • Commercially flexible for the right profile, • Work is starting immediatelywith teams already mobilised How to Express Interest If youre interested or know someone who fits this description wed love to talk. JBRP1_UKTJ

• Clinical Deputy Manager, • Stildon (East Grinstead), • £51,273 per annum, • 35 hours per week, • Extensive CPD programme, • Free meal on shift, • Not for Profit care provider An exciting opportunity has arisen to join Brendoncare as the Clinical Deputy Manager at our care home in Stildon. We are looking for an exceptional clinical nurse leader. The ideal candidate will have strong clinical and leadership skills, a good knowledge of clinical governance, excellent communication skills and the ability to inspire and to lead by example. The Clinical Deputy Manager will join the current home leadership team sharing clinical oversight across the home. They will work with the homes leadership team to support registered nurses and nursing practice On occasion this role will be expected to deputise for the manager and to work in a clinical capacity to support the needs of residents. Essential requirements: • Current NMC registration, • Minimum of 2 years post graduate experience, • Minimum of 12 months in a senior position within a care home setting, • Awareness and understanding of the requirements for a CQC assessment framework, • Experience of advancing frailty, long term conditions and end of life care, • Experience of supporting people living with dementia, • Flexible approach to work with a hands on mindset, • Evidence of continuing professional and clinical development Key Responsibilities: • Assess, plan, implement, and evaluate care plans., • Deliver high-quality care to residents., • Participate in the recruitment of clinical staff., • Support and manage nursing staff through reflective practice., • Develop and oversee nurses' personal development plans., • Provide leadership for the team on a shift-by-shift basis., • Assist nursing staff in collating data, analysing information., • Work proactively with the Home Manager to uphold and enhance nursing standards across the home. Benefits: 6.6 weeks' annual leave increasing to 7 weeks with five years service. In addition we provide training and continuing personal development, a free uniform, free DBS Check, paid breaks, free staff meals when on duty, free on-site parking whilst in the care homes, access to an Employee Assistance Programme, a Refer a Resident Bonus Scheme, and enrolment on to our pension scheme. Who are Brendoncare? Brendoncare is a charity which provides a range of connected services for people in later life including care homes, extra care housing, community support services and clubs across the South of England. We are people-driven, focusing on empowerment, inclusivity and understanding. We aim to ensure that whoever comes into the Brendoncare environment - whether as a member, resident, volunteer or colleague – they are able to live their life to the fullest potential. Our values reflect who we are – together we are kind, empowering, dedicated and forward thinking. We need people who really want to make a difference to the lives of people in later life to join us. In return, we will support you to grow and flourish as you are welcomed to the Brendoncare team. If you are passionate about providing exceptional care and leading a dedicated team, we would love to hear from you! Safeguarding is a core priority for us. All successful candidates will be required to undergo an enhanced Disclosure and Barring Service (DBS) check as part of our commitment to ensuring a safe and secure environment for everyone. Please note: We are running a dynamic recruitment process and may begin interviewing suitable candidates before the closing date. We encourage early applications to ensure consideration. JBRP1_UKTJ

Contract Type: Permanent Hours: Full time Disability Confident: No Closing Date: 26/06/2026 Job summary: The post-holder will manage a caseload and deal with a wide range of health needs in a primary care setting, ensuring the highest standards of care for all PCN patients. Clinical responsibilities: In accordance with the Hub timetable, as agreed, the post-holder will make him/her-self available to undertake a variety of duties including surgery consultations, telephone consultations, checking and signing prescriptions, and dealing with queries, paperwork and correspondence in a timely fashion Making professional, autonomous decisions in relation to presenting problems, whether self-referred or referred from other health care workers within the organisation Assessing the health care needs of patients with undifferentiated and undiagnosed problems Screening patients for disease risk factors and early signs of illness Providing counselling and health education Admitting or discharging patients to and from the caseload and referring to other care providers as appropriate Recording clear and contemporaneous consultation notes to agreed standards Collecting data for audit purposes Compiling and issuing computer-generated acute prescriptions (avoiding hand-written prescriptions whenever possible) Prescribing in accordance with the PCN prescribing formulary (or generically) whenever this is clinically appropriate In general the post-holder will be expected to undertake all the normal duties and responsibilities associated with a GP working within primary care. Jobs are provided by the Find a Job Service from the Department for Work and Pensions (DWP). #J-18808-Ljbffr

The Head of Mechanical and Electrical Compliance is the Trust's strategic and corporate lead for engineering compliance, statutory assurance and infrastructure risk management across all Trust-owned sites. The post holder holds corporate responsibility for ensuring compliance with statutory, regulatory and mandatory requirements relating to Mechanical and Electrical systems, engineering safety, infrastructure resilience and healthcare technical standards, and for providing expert advice on risk acceptance, derogations and mitigation. Operating at senior management level, the role provides strategic leadership, technical policy ownership, delegated financial accountability and expert assurance to Executive Directors and Board-level committees, including leadership of formal audit and inspection programmes and reporting of compliance performance, key risks and residual risk. The post holder develops and delivers the Trust's Engineering Compliance Strategy and annual compliance plan, ensuring safe, resilient and legally compliant estate infrastructure that supports clinical services and patient safety, and driving continuous improvement through risk-based investment, performance management and assurance. Strategic Leadership & Assurance Lead the Mechanical & Electrical compliance function, setting strategy, standards and priorities to maintain a safe, resilient and legally compliant estate. Statutory Compliance & Governance Responsibility for statutory engineering compliance, ensuring robust governance, policies and assurance systems aligned to legislation and HTMs. Risk Management & Reporting Lead infrastructure risk management, including assessment, mitigation and risk acceptance. Provide clear compliance reporting, KPIs and assurance to senior leaders and Board committees. Engineering Strategy & Planning Develop and deliver long-term engineering and infrastructure strategies to support clinical services, patient safety and organisational objectives. Financial & Resource Management Manage compliance budgets and contract performance, ensuring value for money and risk-based prioritisation. Capital & Infrastructure Oversight Provide technical leadership on capital projects and major maintenance, ensuring compliance and resilience from design to operation. Leadership & Workforce Development Develop engineering teams, ensuring competence, training, authorisation and performance management. Emergency Preparedness & Resilience Provide senior support during incidents and lead infrastructure resilience and business continuity planning. Stakeholder Advisory Act as senior technical advisor to executives, clinicians and partners, influencing decisions through clear risk communication. Sponsorship We are an approved sponsoring organisation. Applications will be considered from applicants requiring sponsorship alongside all other applications. Please be aware, not all roles are eligible for sponsorship. You can review the list of eligible role and requirements on the government website. Band 8b Job Purpose The Head of Mechanical and Electrical Compliance is the Trust's senior lead for engineering compliance, statutory assurance, and infrastructure risk management across all Trust sites. This role holds corporate responsibility for ensuring that all mechanical and electrical systems meet statutory, regulatory and mandatory requirements. The postholder will lead the development and delivery of the Trust's engineering compliance strategy, ensuring safe, resilient, and fully compliant estate infrastructure that supports clinical services and patient safety. Operating at senior management level, the role provides expert assurance to Executive Directors and Board-level committees, leading audit and inspection programmes, managing risk, and driving continuous improvement across engineering services. • Lead the Engineering Compliance and Assurance function across all Trust sites., • Develop and deliver a 35 year Engineering Compliance and Infrastructure Strategy aligned to organisational priorities., • Set standards, priorities, and performance expectations for engineering compliance and infrastructure resilience., • Ensure service structures, workforce capability, and succession planning support safe and compliant delivery., • Hold corporate responsibility for statutory compliance relating to mechanical and electrical systems., • Ensure effective governance, authorising arrangements, and safe systems of work are in place., • Develop and maintain Trust-wide policies, technical standards, and compliance frameworks., • Lead a risk-based audit and inspection programme aligned with national guidance and legislation., • Provide formal assurance reporting to senior leadership, including KPIs, compliance dashboards, and risk updates., • Manage engineering risk processes, including mitigation, escalation, and recommendations on risk acceptance or derogation., • Manage delegated engineering compliance budgets, ensuring value for money and alignment to risk priorities., • Oversee contractor performance, expenditure, and delivery of compliance programmes., • Lead engineering input into capital programmes, including business cases, technical approvals, and governance., • Develop long-term lifecycle investment plans based on asset condition, compliance gaps, and risk., • Provide senior leadership to engineering teams and specialist advisors., • Ensure robust competence, authorisation, and training frameworks across engineering disciplines., • Lead recruitment, performance management, and professional development., • Manage complex organisational change within the engineering compliance portfolio., • Provide technical oversight and assurance across capital schemes and major maintenance programmes., • Ensure compliance and resilience requirements are embedded from design through to operation., • Lead engineering input into estate planning, refurbishments, and service developments., • Oversee commissioning, testing, and handover processes, ensuring operational readiness and compliance., • Lead engineering response to major incidents, supporting clinical continuity and escalation to Executive teams., • Oversee resilience planning for critical systems including power, water, ventilation, and medical gases., • Ensure governance arrangements for planned outages and business continuity are robust., • Ability to lead, influence, and engage senior stakeholders across clinical, operational, and technical areas., • Skilled in presenting complex technical and risk information to Executive and Board-level audiences., • Strong negotiation skills, with the ability to manage competing priorities and achieve consensus., • High standards of professionalism, integrity, and confidentiality., • Ability to interpret complex technical, financial, and regulatory information., • Strong data analysis capability, including compliance KPIs, audit outcomes, and incident trends., • Effective programme and portfolio management across multiple competing priorities., • Highly organised, with the ability to adapt in a fast-paced and complex environment., • The role requires occasional travel between Trust sites., • The postholder will be expected to comply with all organisational policies, governance requirements, and statutory obligations. This is a senior leadership role responsible for ensuring that engineering systems and infrastructure are safe, compliant, and resilient. The postholder will play a critical part in safeguarding patient care by managing risk, driving compliance, and shaping long-term engineering strategy across the Trust estate. • Recognised craft apprenticeship or equivalent training and relevant certification, • Degree in Mechanical or Electrical Engineering (or equivalent experience at Masters-level standard). HNC, HND or equivalent in electrical engineering, • Chartered Engineer status or working towards (or equivalent professional standing), • Recognised H&S qualification, • Postgraduate qualification in engineering, estates management or leadership., • Corporate membership of an appropriate body, • Authorised person for specialist NHS HTM disciplines, • Significant senior-level experience leading engineering compliance within a complex healthcare estate., • Experience in devising and managing maintenance systems, establishing and implementing workmanship quality and financial assurance for contracted out maintenance services/in-house estates team/external contractors, • Working within a quality environment, • Experience in the development and management of budgets, • Experience of working in the NHS or similar background, • Experience of working with people from a variety of disciplines, • Experience of strategic infrastructure planning within healthcare., • PFI Experience, • Responsible person water, • Appointed Person electrical LV/HV, • Ability to lead through others, work collaboratively at senior level, and operate with a high degree of autonomy and accountability., • Advanced report writing and assurance skills, including the ability to synthesise complex evidence into clear recommendations and actions., • Digitally competent, able to specify and use performance and assurance information systems (e.g., CAFM, audit tools, reporting dashboards) to support governance and decision-making., • Ability to make high-impact decisions under uncertainty, balancing patient safety, service continuity, regulatory compliance and financial constraints, and escalating appropriately., • High standards of integrity and professionalism, including the ability to provide objective technical challenge and evidence-based recommendations., • Ability to communicate effectively at all levels, including Executive/Board committees and with external auditors/inspectors, translating technical risk into clear options and decisions., • Ability to lead technical investigations and assurance reviews of complex system failures/incidents, identify root causes and commission corrective actions., • Ability to specify, procure and manage complex contracts and service level agreements, holding internal and external providers to account for delivery and compliance., • Ability to interpret, quality assure and present complex performance and risk data (dashboards, audit outcomes, incidents, compliance trajectories) to inform executive decisions., • Ability to chair governance meetings and lead performance reviews with contractors and internal teams, providing robust challenge and agreement of remedial actions., • Strategic problem-solving skills, including options appraisal and recommendation of proportionate solutions in a complex risk environment., • Resilient leader, able to remain effective under pressure, including during incidents and periods of heightened regulatory scrutiny., • Ability to manage a complex portfolio of work, prioritising based on risk and organisational impact, and ensuring appropriate governance and documentation., • Surveying (M&E, Construction) skills., • In depth knowledge and understanding of DoH technical guidance, statutory instruments and industry best practice in regard to healthcare estates services., • Excellent project management skills including an ability to lead on projects which may be uncertain and subject to constant change., • Commitment to Continuing Professional Development (CPD)., • Values and respects others, treats everyone as an individual, is non judgemental., • Motivated to be genuinely kind and caring., • Helps and co-operates with colleagues., • Pro-active and takes responsibility., • Willing to learn open to change., • Motivated to make a difference in whatever way they can., • Takes pride in themselves, their appearance, their role and where they work., • Actively supports the Trust's values., • Willing to travel occasionally between Trust community sites This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Alder Hey Children's NHS Foundation Trust Alder Hey Children's NHS Foundation Trust #J-18808-Ljbffr

Reporting to the Site Head of Quality Assurance, the Head of Front Line QA (and QP, if eligible) provides independent QA/QP oversight for all operations at Seqirus Liverpool, as well as support to commercial affiliates and contract manufacturers per approved Quality Agreements. The role leads and develops the Front Line QA function to ensure pharmaceutical quality across all products manufactured, tested, distributed and/or released at the site, ensuring compliance with all regulatory, quality and internal requirements. When acting as a QP (if eligible), the role holder is responsible for certification and release of commercial and clinical products, and for oversight of intermediate product release throughout the manufacturing process. The Head of FLQA shapes site quality culture and strategic direction, ensuring robust quality systems and standards are in place and effectively applied in alignment with regulatory expectations. The role holder is responsible for providing direct Quality oversight across all Manufacturing, QC, Engineering and supporting operational areas. This includes Quality support for projects, initiatives, and routine activities associated with all GMP operations on site. They lead a team that delivers 24/7 QA coverage to Primary and Secondary manufacturing, ensuring continuous quality presence and timely decision‑making to maintain compliant and efficient operations. The role is accountable for the site processes governing QA Batch Review and QA IT, ensuring these systems are robust, effective, and fully aligned with applicable regulations, cGMP requirements, and current industry best practice. The role holder is responsible for certification and/or rejection of product destined for release to market in compliance with applicable licences and legal requirements. The role holder must maintain eligibility to act as a QP by completing Continuous Professional Development (CPD). • QA Leadership, • In conjunction with the Site Head of Quality Assurance, the role holder provides strong leadership and strategic direction to the Quality Assurance team, mentoring and developing staff both technically and professionally (and if an eligible QP, including acting as a sponsor for trainee QPs). Nurturing a high‑performing team of quality professionals by clearly defining expectations, holding individuals accountable, managing prioritisation/workload allocation, recognising accomplishments, managing performance, and ensuring professional development., • Actively promotes and maintains a cGMP compliant culture, ensuring that the highest standards of quality, housekeeping, and safety are applied within the team. The role holder will be an official delegate for the Site Head of Quality Assurance., • The role holder supports the management and development of the Pharmaceutical Quality system (PQS), including Management Review, ensuring compliance with regulatory requirements, company procedures and industry best practice., • The role holder ensures that quality systems consistently support compliant product release, reliable data integrity, and sustained inspection readiness across the site., • As a leader within Quality Assurance, the role holder must establish quality objectives and associated Key Performance Indicators (KPIs) for the Front Line QA function and must ensure that these objectives are met. Provide QA/QP (if eligible) oversight of all site operations, and to contribute effectively to the strategic development of company systems. Directly responsible for ensuring implementation and use of Quality Systems for GMP areas in the facility, such as DR/CAPA management, Change Management, document management and training systems. Locally, the QP (if eligible) must provide oversight of key site meetings / publications, such as Local Quality Management Review, Deviation Review Board, Change Review Panel, Site Stability Meeting, Continuous Process Verification, Campaign Management meetings and regulatory planning meetings. In addition to local responsibilities, the role holder must integrate with External Supplier Quality, Supply Chain QA and Contract Manufacturing QA management to provide oversight of GMP suppliers, third‑party distributors and contract manufacturing operations. Support and guidance must be given relating to key quality decisions impacting the manufacturing and movement of in‑process, quarantined and fully released product under the QP’s responsibility. Develop and maintain a relationship with regulatory authorities (e.g. Health Authorities and Official Medicines Control Laboratories), including participation in the inspection process site audits as appropriate and oversight of BPDRs/notifications. Acquire and maintain knowledge of local and international regulatory and legislative requirements for pharmaceutical current good manufacturing practices and trends for all markets to which the site distributes product and utilise this knowledge to implement improvements at the site. Drive adherence to and continuous improvement of the quality systems within their areas of oversight. Interact with the Regulatory department to maintain QA oversight of new product licence submissions and variations. The Head of Front Line QA (and QP, if eligible) is expected to act as a host and/or lead presenter, as required, during regulatory inspections. • Degree in science related field and/or relevant experience, • Postgraduate qualification preferred, • Eligible Qualified Person (QP) preferred, • 5 years experience in a QA leadership role, preferably with experience in Sterile manufacture. Benefits information available at _. CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit _. #J-18808-Ljbffr

Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry's most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions. Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases. At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients' lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law. The primary purpose of this role is to contribute to cross functional efforts focused on applying the ImmTAX platform or other modalities to the development of novel treatments for chronic infections, including HIV and HBV and EBV-associated diseases. The team is involved in multiple stages of the drug discovery and development process, from target discovery all the way to clinical trials. Examples of key preclinical research are published in Yang H et al., Mol Ther. 2016; 24,11; Fergusson J et al., Hepatology 2020; 72,5; Wallace Z et al., Mol Ther 2024; 32, 678. The postholder will plan, design and execute experimental investigations to support the advancement of the Company pipeline, processes and technology capabilities, with guidance from their manager, ensuring that project goals are met within time and budget constraints. They will be expected to demonstrate technical proficiency, rigour in assessing their own data and that of others, scientific creativity and independent thought. This position requires participation and presentation of results at internal meetings, sharing information learned at external scientific meetings and establishing productive relationships with colleagues across Research and other departments. Key Responsibilities: • With instruction and guidance from manager - plan, design, and execute assignments to meet project goals within defined timeframes, • Execute experiments to address key scientific questions and enable project progression, utilizing range of molecular and cellular techniques including some of the following: NextGen sequencing, DD-PCR, qPCR, cell culture, flow cytometry, ELISpots, ELISAs,, • Some work will be conducted in a containment level 3 (CL3 facility) and will require handling of human viruses, • Analyse data, interpret results, and make recommendations, • Proactively expand scientific/technical knowledge in relevant fields including HIV/HBV/EBV related disease biology and drug development through review of scientific literature/ conference updates, peer to peer mentoring, and attendance at seminars/conferences in line with company strategy, • Work effectively in a matrixed team structure and as part of cross functional teams, • Participate and present results at internal meetings, • Establish relationships and possible collaborations within and outside of the company Education, Experience and Knowledge: Essential Qualifications: • PhD in molecular biology, cell biology, genomics, virology, immunology, or related discipline and 0-2 years related experience, • Alternatively, a BSc or MSc with significant work experience in relevant scientific areas, • Worked in a bench-based laboratory environment and proficient inthe following key techniques: o molecular techniques including some of the following: Droplet Digital PCR, NextGen sequencing, Genomics/Transcriptomics, PCR, Mutagenesis, qPCR o Culturing primary cells and/or cell lines Preferred Qualifications: • Knowledge/expertise of Immunology/HIV/HBV/EBV, • Flow cytometry, ELISAs, ELISpots, • Viral integration site analysis

Leading clinical quality improvement through insight, collaboration and targeted development to enhance performance and patient care. Clinical CQI & DoS Lead At DHU Healthcare, every role matters. Because every moment gives us the chance to make the difference - for patients, colleagues and communities. Wherever you join us, your compassion, commitment and skills will not only make all the difference in the moment today but also shape the care we deliver tomorrow. DHU Healthcare has been providing the support patients need for more than 30 years. Today, we're proud to be the largest NHS 111 provider in the country, rated OUTSTANDING by the Care Quality Commission. Our teams answer around one in every four NHS 111 calls made across England, providing millions of people with safe, compassionate advice when they need it most. Key Responsibilities • Maintain expert knowledge of NHS Pathways through regular call taking, ensuring safe, effective and patient-centred decision making., • Lead and support Clinical Quality Improvement (CQI) processes, using audit, data analysis and patient journey reviews to drive continuous improvements in care quality and outcomes., • Work collaboratively with internal teams and external partners to review calls, share learning and improve patient journeys across the wider healthcare system., • Support the investigation and management of incidents and complaints, producing clear reports, identifying themes and embedding learning to enhance service delivery., • Analyse quantitative and qualitative data to identify risks, trends and opportunities, presenting insights to inform governance, decision making and service improvement., • Develop, implement and maintain robust processes, procedures and audit trails in line with governance and ISO standards., • Design and deliver targeted training, coaching and mentorship to improve individual and team performance, fostering a culture of continuous learning., • Work closely with managers and trainers to identify performance trends, address outliers and support staff development and capability., • Ensure quality and consistency of NHS Pathways training through audit and ongoing support to trainers., • Contribute to stakeholder engagement with professionalism, building strong working relationships across systems., • Provide regular updates to senior leadership on CQI progress, KPIs and improvement initiatives., • Support the effective use and development of the Directory of Services (DoS), analysing performance, identifying improvements and collaborating with regional and national teams to enhance service delivery., • Lead or support service improvement initiatives, system testing and implementation projects, including NHS Pathways and Adastra developments., • Maintain accurate documentation and support business continuity processes, escalating risks where required., • Uphold professional standards, maintaining registration, accountability and compliance with regulatory requirements., • Registered Clinician accreted to use NHS Pathways Clinical Decision Support Software., • Accredited NHS Pathways Coach or Trainer. With us, your wellbeing comes first. We'll support your health, happiness and future with benefits that put you first: • Access to the NHS pension scheme (we'll also honour your existing NHS pension pot and holiday entitlement if you're transferring), • Wellbeing support, • Flexible working options, • Career growth and development opportunities For more information on the full range of benefits available click here . Enjoy the same great benefits as you move into your new role. Enjoy the same great benefits as you move into your new role. Your benefits continue with you, supporting your health, wellbeing, and future. For more information on the full range of benefits available, click here . Keep developing as you step into your new role Keep developing as you step into your new role Your development moves with you with us, you can continue building your skills and exploring new opportunities. With career pathways, tailored training, and the DHU Academy, you'll have the tools and encouragement to take the next step, make an impact, and grow in ways that matter to you. With us, everyone belongs. Great work happens when everyone feels seen, supported, and valued. We welcome colleagues from all backgrounds and proudly support the Armed Forces community. Inclusion and belonging are essential to our values, and together we make the difference. As a Disability Confident Employer, we welcome candidates to share any support or reasonable adjustments they may need during the recruitment process. For more information on how DHU can support you, please click here . Your skills, ideas, and growth continue to matter at DHU Healthcare. Take the next step and make an even greater impact. #IND1 JBRP1_UKTJ

We are a busy organisation that consists of multiple GP surgeries in Liverpool. With over 120 staff members, our focus is to develop and nurture our staff. We reward positivity, innovation and hard work. We are looking for a Practice Doctor to join our friendly, hardworking and forward-thinking team. You will be located in one of our Liverpool-based surgeries along with the opportunity to operate on a cross-site basis. The ideal candidate will have practice experience. To be responsible for the delivery of practice services, working as part of the practice multidisciplinary team, delivering care within their scope of practice to the entitled patient population. We are looking for an enthusiastic and motivated doctor, committed to delivering outstanding care to our patient population. You would be working as part of a friendly, team spirited group of professionals committed to providing the best service for our patients. This is an exciting time to join our organisation and this role is integral to our approach to patient care. Enthusiastic about General Practice A team player Innovative Wants to work with a proactive and forward thinking team We are an organisation that is built on providing the best medical care and treatment in a friendly and comfortable environment. We are a fast- paced clinical organisation.We have highly skilled clinical staff providing both reactive and proactive care, along with skilled administration and management teams who provide essential support. We take great pride in being an open, trusting and compassionate organisation. We are committed to promoting and building a team that enhances inclusion, diversity and equality. In accordance with the current access model, the post-holder will make themselves available to undertake a variety of duties, including surgery consultations, telephone consultations and queries, visiting patients at home, checking and signing repeat prescriptions and dealing with queries, paperwork and correspondence in a timely fashion Making professional, autonomous decisions in relation to presenting problems Assessing the health care needs of patients with undifferentiated and undiagnosed problems Screening patients for disease risk factors and early signs of illness Developing care plans for health in consultation with patients and in line with current practice disease management protocols Recording clear and contemporaneous consultation notes to agreed standards Collecting data for audit purposes Compiling and issuing computer-generated acute and repeat prescriptions (avoiding hand-written prescriptions whenever possible) Prescribing in accordance with the practice prescribing formulary (or generically) whenever this is clinically appropriate In general, the post-holder will be expected to undertake all the normal duties and responsibilities associated with a GP working within primary care. • Bachelor's degree in medicine (MBBS) or surgery (BMBS) that has been recognised by the General Medical Council (GMC)., • Experience of using Emis Web, • Ability to provide quality care Good interpersonal and communication skills Awareness of and compliance with all relevant practice policies/guidelines, e.g. prescribing, confidentiality, data protection, health and safety Attending training and events organised by the practice or other agencies, where appropriate., • Contributing to evaluation/ audit and clinical standard setting within the Practice. This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. #J-18808-Ljbffr

Following the retirement of our Chief Nurse, we are seeking an exceptional and accomplished leader. The successful candidate will be an existing Chief Nurse or an experienced Deputy Chief Nurse from a comparable organisation, ready to lead nursing and Allied Health Professionals across our organisation and its distinctive model of care. As Chief Nurse and Executive Director at one of the UK's leading cancer centres, the post holder will play a pivotal role in shaping and delivering the Trust's nursing and AHP strategy, driving quality, efficiency, and sustainable improvement in clinical services and patient experience. As a key member of the Executive Team, this is an opportunity to build on the excellent work that underpins our success. You will bring credibility, presence, and ambition, inspiring confidence and influencing colleagues at every level. You will quickly build trusted relationships with staff, patients, partners, regulators, and communities, champion our values, and foster behaviours that keep patients at the centre of everything we do. As a visible and inclusive leader, you will empower our nursing and AHP workforce, uphold professional standards, and drive continuous improvement. You will bring a strong track record in workforce development and service improvement, with the ability to drive high performance, hold others to account, build cohesive teams, and inspire excellence. A passion for excellent patient care, together with a strong commitment to population health, inclusion, and reducing health and race inequalities, will be essential. Resilience and determination will be important in navigating challenges and making a positive, lasting difference. • Registered nurse with current NMC registration, • Educated to degree level, ideally masters, or equivalent experience, • Significant senior nursing leadership experience within a complex healthcare organisation ideally at Board-level or equivalent responsibility, • Proven record of improving patient safety, clinical quality, patient experience and outcomes at scale, including measurable quality improvement, • Experience of leading services through change, including service redesign and transformation, while maintaining safe care and staff engagement, • Demonstrated ability to provide operational grip and professional leadership, using data and insight to improve quality and workforce performance, • Experience of championing professional standards, patient involvement, and equality, diversity and inclusion in care and workforce, • Evidence of leading high‑performing nursing and multidisciplinary teams and developing positive organisational cultures, • Successful partnership leadership across complex systems and diverse communities, influencing improvement beyond organisational boundaries, • Experience of delivering transformation, innovation and quality improvement, including embedding improvement methods and capability, • Experience of managing resources and contributing to financial stewardship through safe, effective workforce deployment and service improvement, • Experience of leading and assuring clinical governance, risk management and response to serious incidents, working closely with senior clinical leaders, • Deep understanding of national and local quality, patient safety and nursing policy and the context for specialised and cancer services within the NHS, • Strong appreciation of population health, inequalities and community needs, and how nursing leadership can help reduce unwarranted variation, • Significant knowledge of effective clinical governance and assurance frameworks, including CQC standards, safeguarding, IPC and quality reporting, • Understanding of education and academic partnerships, research participation and innovation in nursing and clinical care, • Strategic leadership capability with the ability to translate Trust strategy into deliverable operational plans and measurable outcomes, • Strong performance management and improvement skills, including the ability to use data, assurance reporting and predictive insight to drive quality improvement, • Visible, inclusive and compassionate leadership style that promotes an open culture, empowers teams and role models high professional standards with authenticity as a values‑driven professional nurse leader, • High level influencing and stakeholder management skills with credibility to represent the Trust, • Ability to develop leadership capability and talent, including succession planning and performance development, • Highly credible communicator with political acumen and emotional intelligence, able to influence at Board and system level, • Courageous and decisive, with the ability to challenge appropriately and act on quality and safety concerns, • Commitment to equality, inclusion and to reducing health and workforce inequalities through population health approaches including compassionate leadership and anti‑racist practice, • Collaborative, curious and open, with strong accountability and a commitment to learning and improvement, • Inspires confidence, ambition and pride in nursing and multidisciplinary teams, and builds trusting relationships with patients and partners, • Resilience and personal effectiveness to operate in a high profile, high‑accountability role, managing competing priorities and delivering through others This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and, as such, it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Permanent Full‑time 158-26-094-EXE The Clatterbridge Cancer Centre - The Spine #J-18808-Ljbffr

Welcome to FCMS! Fixed Term Contract until April 2027 Post:Practice Nurse / Community Outreach Target Demand Management (TDM) Pay: £19.78-£20.88 dependent on experience Hours: Full, Part and Bank Hours Available Accountable to: Head of Clinical Workforce Reportable to: Clinical Manager Base: Work will be undertaken on our Mobile Unit with a base of Newfield House, Vicarage Lane, Blackpool, FY4 4EW Closing Date: 6th July 2026 Please note that our roles are not being considered for sponsorship at this time Overview of Role: At FCMS we provide several services across the Fylde Coast, Morecambe Bay, Rossendale, West Lancashire and Doncaster as well as diagnostic services across the country. These include GP Out of Hours services, Urgent Treatment Centres, and range of other Primary Care Services including Enhanced Access (Fylde Coast) and Special Allocation Services (Lancashire / Cumbria/Parts of Cheshire and Merseyside). TDM supports people across Blackpool to address clinical and non-clinical factors increasing their risk of an unplanned hospitalisation. Based on the evidence-base there is an underlying risk factor of socio-economic disadvantage which means that more support delivered through non-traditional mechanisms is required to improve health outcomes. Key aims of TDM are to provide clinical and non-clinical interventions that meet the needs of individuals identified in Blackpool through a mixed case-finding approach including the Core20Plus5 cohorts and with the following Long-Term Condition - cardiovascular disease (CVD) and/or COPD. The aim is to support them to achieve their maximum potential for physical, cognitive, social and psychological function, participation and quality of living. To achieve all these goals, we will be working collaboratively with other Blackpool Based organisations such as Healthwatch, PCN Social Prescribers, Community Nursing and Housing Intervention teams. Main duties of the job We are looking for motivated clinicians to deliver high-quality, patient-centred nursing care within the heart of the community on our mobile unit. The role focuses on patients with long term conditions, particularly cardiovascular disease (CVD) and COPD within the core20plus5 cohorts. The postholder will provide holistic clinical and non-clinical interventions aimed at improving physical, cognitive, reducing health inequalities and preventing health crisis. About us The ethos of FCMS as a social enterprise, health and wellbeing services provider is to be passionate in its drive to ensure that patients and callers remain the central focus of all that it does. Coupled with excellent and well-established clinical governance systems and extremely effective operational expertise, it has meant that the company has the ability to strategically visualise, develop, and implement award winning services. Over many years we have invested in our staff so that we have a core team of highly trained individuals who can manage the needs of our patients and callers. Our staff are able to significantly improve the service delivery and user experience due to their considerable experience and commitment to what they do. Come and be a part of our amazing team! We offer NHS Pension Cycle to Work Scheme Career Development Opportunities Attendance Bonus Staff Benefit Scheme Free Tea & Coffee Eye Care Contributions Day to Day Duties to include, but not exhaustive: To provide proactive reviews and support for patients with CVD and / or COPD in line with clinical competence and local pathways Undertake holistic health assessments, identifying physical, mental and social needs Deliver health prevention and health promotion interventions including lifestyle advice (alcohol, smoking, diet and physical activity), weight management and wellbeing support, Opportunistic screening and vaccination advice Identify unmet needs and escalating health concerns, taking appropriate actions Deliver care within the mobile clinical unit adapting consultations to a community-based environment Support people who present to the mobile unit by providing assessment and advise where appropriate, signposting and referring to the most suitable service when out the scope of practice and offering reassurance, health information and ongoing support Promote self-management and empower patients to engage with health services Accurately record all activity, assessments and outcomes on EMIS using appropriate clinical coding and templates Maintain confidentiality and data protection standards Maintain Current NMC registration adhering to the NMC code of conduct Work autonomously withing scope of practice, escalating concerns appropriately Participate in supervision, appraisal and continuing professional development Contribute to service development, evaluation and quality improvement initiatives Multidisciplinary Working Work collaborativelywith other Blackpool Based organisations such as Healthwatch, PCN Social Prescribers, Community Nursing, Housing Intervention teams. Our key expectations are: Self-awareness Living authentically Adaptability- Being ready to adjust depending on the situation Openness What you see is what you get Positivity with a real sense of being able to strive for the impossible Generosity of spirit- Everyday should be an opportunity to act with kindness Ability to have fun Taking the role seriously, whilst being yourself Our Why:To nurture an environment of inspiration, innovation and disruption so this people in our world receive exceptional healthcare for this generation, and the next. Values:Our organisational culture is very important to us, so it is vital that the successful candidate lives and breathes complimentary values and behaviours. Our behaviours should be in line with our values which form part of our Company DNA: Fun:People rarely succeed unless they are having fun. Happiness is healthy! Awesome:We arent here to be average, were here to be awesome! Humble:Were here to make a difference to the lives of others, NOT to see how important we can become Brave:We challenge the norm. We have the courage to get the difficult jobs done Oompf:We have natural oompf! Its infectious! Go-getting:We are intuitive to changing needs and respond quickly which we do with energy, ideas, and positivity Come and be a part of our amazing team! We offer NHS Pension Cycle to Work Scheme Career Development Opportunities Attendance Bonus Staff Benefit Scheme Free Tea & Coffee Eye Care Contributions Disability Confident Employer As users of the disability confident scheme, we guarantee to interview all disabled applicants who meet the minimum criteria for the vacancy DBS -This post is subject to the Rehabilitation of Offenders Act (Exemption Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. This will require three forms of valid ID to be produced and verified. The onboarding process is also subject to an Occupational Health check, suitable professional references and eligibility to work in the UK (with the requirement to provide relevant documentation as evidence).For Driver positions you will also be required to undertake a Driver check. The organisation is committed to safeguarding and promoting the welfare of children, young people and vulnerable adults and expects all staff to share this commitment. You will be expected to fulfil your mandatory safeguarding training at the level applicable to this role. We reserve the right to close this vacancy early if we receive sufficient applications for the role. Therefore, if you are interested, please submit your application as early as possible. Person Specification Personal Qualities Essential • Willing / able to attend appropriate training, • Commitment to own personal development, • Able to exercise initiative in organisation and prioritising, • Good communication skills both written and oral, • Good Interpersonal skills, • Basic IT skills Enthusiastic and committed about the role, • Flexible, • Promote the Service with its ever expansion, • Knowledge of current clinical and professional issues Desirable • Willing to try new IT systems in the future for consultations Experience Essential • Long Term Condition Monitoring, • Working in Primary Care / GP Practice, • Ability to use EMIS computer system, • Health Promotion, • Understanding of health inequalities and the core20Plus5 priorities Desirable • Experience of a multi-disciplinary approach to working, • Experience in case management, • Experience of working with socioeconomically disadvantaged populations Qualifications Essential • Registered Nurse, • NMC, • 2 years post qualification, • Long term condition qualifications Respiratory, CVD, • Venepuncture, • Feno Testing, • Spirometry accreditation Desirable • NMP v300 prescriber, • Other Long Term Condition qualifications Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. UK Registration Applicants must have current UK professional registration. JBRP1_UKTJ

Company description: Vitaflo (International) Limited For more than 25 years, Vitaflo has developed innovative specialised clinical nutritional products for inherited metabolic disorders, pediatric?kidney disease, and specialised diets such as the ketogenic diet. Vitaflo products offer patients choice, flexibility, and convenience. We combine the latest medical research, together with insights on changing modern lifestyles to best support patients in the compliance of restrictive therapeutic diets. Vitaflo continues its mission of Enhancing Lives Together with research and development at the heart of what we do. Job description: We are part of Nestlé Health Science and continue to expand our global footprint with a worldwide presence in Clinical Nutrition. Behind our pioneering company are people who drive breakthroughs in research and development, creating innovative impact. Our employees are at the heart of what we stand for with 96% saying they are proud to work for us and 94% recommending Vitaflo as a good place to work. Our Headquarters, based in Liverpool, is the hub of innovative and creative activity. We strive to be at the cutting edge of our industry sector with patients needs being at the forefront of our mind. We work collaboratively, share our knowledge and expertise and above all love what we do and why we do it. We are currently looking to recruit a Paralegal on a full-time basis for an 18-month fixed term contract, based at our Liverpool Headquarters. Reporting to the Head of Legal, you will help to deliver a responsive, business-facing legal service across multiple areas of the business. This is an excellent opportunity for a commercially-focused paralegal looking to develop broad in-house experience in a busy team of two solicitors. Vitaflo operates a hybrid working policy, subject to role requirements and business needs. What will you do? As a Paralegal, your main responsibilities will be Contracting & Transaction Support • Draft, review and manage a range of standard commercial agreements (e.g. NDAs and service agreements), • Support contract lifecycle management, including execution, storage and tracking, • Maintain and update legal templates and databases Legal Operations & Process Efficiency • Support the operation and implementation of legal systems and tools (e.g. contract management, e-signature platforms), • Assist with improving legal processes to enhance efficiency and consistency, • Maintain organised legal records and ensure robust audit trails Business support • Act as a first point of contact for routine legal queries from internal stakeholders, • Work closely with Commercial, R&D, Supply Chain, Finance and HR teams to support day-to-day legal needs, • Support training and guidance to the business on legal and compliance matters, • Maintain the international registered trade mark portfolio, with support from Vitaflo's parent company, ensuring alignment with brand managers Compliance Support • Advise and support employees to comply with relevant laws and internal policies (e.g. business integrity, GDPR), • Support the ESG officer with initiatives (e.g. DEI, sustainability compliance, PPWR) and related audits. Administrative Support • Coordinate with external counsel where required, • Support work planning, budgeting and invoice management Who are we looking for? You will have: Essential skills/experience • Previous experience in a paralegal or legal assistant role (in-house or private practice), • Strong understanding of commercial contracts, • Highly organised, with excellent attention to detail and ability to manage multiple priorities, • Strong stakeholder management and communication skills, • Confident using legal technology and Microsoft Office tools Desirable skills/experience • Experience of intellectual property law, • Knowledge of the healthcare or pharma sectors What we offer? • Competitive salary, • 25 days annual leave (pro rata for part time) plus bank holidays and Christmas shut down, • Discretionary bonus scheme (subject to qualifying period), • Gym membership/allowance (subject to qualifying period), • Employer pension contribution (3% rising to 5% subject to qualifying period then matched to a maximum of 10%). Employee minimum contributions apply, • Private healthcare (subject to qualifying period), • Volunteering opportunities, • Cycle to work scheme (subject to qualifying period) At Vitaflo (International) Ltd, our values are rooted in respect - for our employees, our customers and our patients. That's why championing diversity and inclusion is so important to us; when we embrace different perspectives and give everyone the chance to be the best they can be, we can think in new, creative ways that grow and enhance our business. We are committed to equal opportunity for all, and we may collect relevant anonymized data for monitoring purposes during our candidate registration process. JBRP1_UKTJ

Occupational Therapist Salary: £42,000-£52,000 per annum (pro rata) Hours: 37.5 hours per week Monday to Friday Location: Various About the Role We are seeking an experienced and motivated Occupational Therapist to join our clients Community Equipment Service (CES) team. This is a varied and impactful role where you will work closely with senior management, commissioners, referrers, and operational teams to deliver a person-centred equipment service. You will play a key role in ensuring individuals have timely access to the right equipment, while driving efficiency, sustainability, and best practice across the service. This is an excellent opportunity for a clinician with strong clinical expertise, service development experience, and a passion for improving outcomes through innovative equipment solutions. What you'll do • Provide specialist clinical advice to CES prescribers on:, • Appropriate equipment provision, • Clinical reasoning, risk management and safeguarding, • Catalogue use and service pathways, • Review and authorise specialist equipment orders, maximising use of recycled special equipment (RSPs) to ensure value for money., • Support and develop clinical governance, prescription criteria, policies and procedures in line with national guidance., • Contribute to the development and review of the TCES equipment catalogue, including identifying Close Technical Equivalents (CTEs)., • Deliver training, familiarisation and equipment demonstration sessions for prescribers., • Undertake audits, service improvement projects and data analysis to reduce risk, improve efficiency and generate savings., • Work collaboratively with CES managers, commissioners, health and social care professionals and suppliers to improve future equipment provision. What We're Looking For: • Degree or Diploma in Occupational Therapy, • HCPC registration, • Significant post-qualification experience at a senior level, • Strong experience within Community Equipment Services, • Knowledge of clinical governance, legislation, and equipment provision, • Excellent communication, analytical, and organisational skills, • Full UK driving licence Your Benefits: • HCPC Registration fees paid, • 33 days annual leave (including bank holidays), • Company pension scheme, • RCOT Membership, • Structured training and development opportunities, • Annual appraisal and career development planning Why sjb medical? sjb medical's vision is simple yet unique: to bring search and selection, and medical expertise together to provide a unique resourcing service to the healthcare sector. We take pride and great care in providing our healthcare candidates with the best possible support throughout their recruitment journey. We understand that a diverse workforce is essential to our clients' success and promotion of equality, diversity and fairness in our recruitment process is paramount. For more information and to apply, please click the apply button. #medical0123 JBRP1_UKTJ

Team Leader (Medical Centre) Location:Liverpool Hours:Full-time, 37.5 hours per week (MondayFriday, 8:00am6:00pm with one late evening) Salary:£29,250 per annum (equivalent to £15.00 per hour) ---------------------------------------- About the Role We are working in partnership with a well-established GP practice in Liverpool who are looking to appoint an experienced and motivated Team Leader to join their management team. This is an excellent opportunity for someone with strong leadership skills and extensive EMIS Web experience to take on a key role in ensuring the smooth, efficient, and professional running of the practices daily operations. The successful candidate will lead and support the reception and administrative teams, fostering a positive and patient-focused culture within the surgery. ---------------------------------------- Key Responsibilities • Lead and supervise the reception and administrative teams, providing training, guidance, and ongoing support., • Manage staff rotas and ensure adequate cover across surgery opening hours., • Oversee daily workflows, ensuring the smooth operation of front-desk and back-office functions., • Use EMIS Web confidently for appointments, reporting, and problem-solving., • Support the Practice Manager with audits, data reporting, and performance monitoring., • Handle escalated patient queries and complaints in a professional and empathetic manner., • Monitor and improve patient access and service quality., • Uphold all confidentiality, information governance, and safeguarding standards. ---------------------------------------- Essential Requirements • Proven leadership or supervisory experience within a GP practice or primary care setting., • Strong working knowledge and confidence with EMIS Web., • Excellent organisational and communication skills., • Ability to manage a busy workload and adapt to changing priorities., • Professional, supportive, and proactive approach to teamwork., • Strong IT skills, including Microsoft Office and NHS systems. ---------------------------------------- Desirable • Knowledge of QOF, recalls, and clinical reporting., • Experience with patient triage systems and online access tools (e.g. AccuRx, eConsult)., • Understanding of NHS policies, compliance, and performance targets. ---------------------------------------- If you have the relevant experience and are looking for your next leadership opportunityplease apply online today our team will be in touch to discuss your application. JBRP1_UKTJ

Liverpool Practice Vacancy: Dunstan Village Group Practice. Seeking to employ a Full or Part time Salaried GP. • List size approximately 8000, • 2.5 full time GP equivalent, • Nursing team includes ANP, Nurse Practitioner and Practice Nurses, • Highly efficient and friendly administrative staff, • Integrated PCN Clinical Pharmacists, Physician Associates, 1st Contact Physiotherapists, Mental Health Team and Social prescriber Start date ASAP, prepared to wait for the right candidate. Salary negotiable depending on experience and additional qualifications/interests. Variety of duties including surgery consultations, telephone consultations, queries, home visits, repeat prescriptions, paperwork and correspondence. In general, the post-holder will be expected to undertake all normal duties and responsibilities associated with a GP working within primary care. The post-holder will manage a caseload and deal with a wide range of health needs in a primary care setting, ensuring the highest standards of care for all registered and temporary patients. Clinical responsibilities: • Make themselves available to undertake surgery consultations, telephone consultations, queries, and home visits as per the practice timetable., • Check and sign repeat prescriptions and handle queries, paperwork and correspondence in a timely fashion., • Make professional, autonomous decisions regarding presenting problems., • Assess health care needs of patients with undifferentiated and undiagnosed problems., • Develop care plans in consultation with patients in line with current practice disease management protocols; manage acute and chronic disease., • Provide counselling and health education., • Admit or discharge patients to and from the caseload and refer to other care providers as appropriate., • Record clear and contemporaneous consultation notes to agreed standards., • Compile and issue computer-generated acute and repeat prescriptions, avoiding hand‑written prescriptions when possible., • Prescribe in accordance with the practice prescribing formulary (or generically) when clinically appropriate. Practice CQC regulated activities: • Diagnostic and screening procedures for disease risk factors and early signs of illness., • Maternity and midwifery services., • Treatment of disease, disorders or injury. Other responsibilities within the organisation: • Awareness of and compliance with all relevant practice policies/guidelines, e.g. prescribing, confidentiality, data protection, health and safety., • Commitment to lifelong learning and audit to ensure evidence‑based best practice., • Contribute to evaluation/audit and clinical standard setting within the organisation., • Contribute to the development of computer‑based patient records and summarising of patient records and read‑coding patient data., • Attend training and events organised by the practice or other agencies, where appropriate., • Health and safety responsibilities., • Equality and diversity., • Extended access shifts on a rota basis. Confidentiality: In the course of seeking treatment, patients entrust us with sensitive information in relation to their health and other matters. They expect staff to respect their privacy and act appropriately. The post-holder may have access to confidential information relating to patients, carers, practice staff and other healthcare workers, and must regard all such information as strictly confidential. The post-holder will implement and lead on a full range of promotion and management of health and safety and infection control for themselves and others, as defined in the practice policies and published procedures. Duties include: • Using personal security systems within the workplace according to practice guidelines., • Aware of national standards of infection control and cleanliness and regulatory and contractual requirements., • Advising on safe specimen handling, labelling, storage and transport., • Correct personal use and oversight of PPE., • Managing all incidents of accidental exposure., • Implementing infection control protocols across the practice., • Observing current working practices, identifying weaknesses or training needs, and escalating issues as appropriate., • Managing risks involved in work activities and preparing mitigation plans., • Utilising training to update knowledge and skills, and training others where required., • Monitoring practice facilities and equipment for infection control compliance., • Ensuring proper use of hand‑cleansing facilities and supplies., • Managing sharps, storage, disposal and maintaining a clean working environment., • Demonstrating regard for safeguarding and promoting welfare of children., • Reporting and correcting health and safety hazards promptly., • Undertaking periodic infection control training at least twice annually. The post-holder will support equality, diversity and rights of patients, carers and colleagues by: • Acting in a way that recognises importance of rights, consistent with practice procedures and policies., • Respecting privacy, dignity, needs and beliefs of all individuals., • Behaving welcomeingly and non‑judgmentally, respecting circumstances, feelings and priorities. Participation in an annual individual performance review, maintaining a record of personal and professional development, and demonstrating skills and activities to peers. The post-holder will maintain quality by: • Alerting team members to quality and risk issues., • Assessing own performance and taking accountability for actions., • Contributing to team effectiveness by reflecting on activities and suggesting improvements., • Managing own time, workload and resources effectively., • Collaborating with individuals in other agencies to meet patient needs. The post-holder should recognise the importance of effective communication within the team and will strive to: • Communicate effectively with team members, patients and carers., • Adapt communication methods to meet alternative needs. The post-holder will: • Apply practice policies, standards and guidance., • Discuss with team members how policies and guidelines affect own work., • Participate in audit where appropriate., • GP This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and requires a Disclosure and Barring Service check to verify any previous criminal convictions. #J-18808-Ljbffr

Laurences Medical Centre is seeking a Receptionist to join our dedicated team in Knowsley, England.The role requires managing patient interactions, appointment systems, and data entry while providing essential support to the clinical team.The ideal candidate will possess strong communication skills,

Because of our unique model, our Medical Assistants oversee the full spectrum of the patient experience- acting both as a Medical Receptionist as well as assuming clinical responsibilities of a Medical Assistant. Records accurate and pertinent data in the medical record according to documentation gu

Job Title: Data Entry Clerk Work From Home - Remote Panelists Part-Time Focus Group Participants - Remote Work From Home (Up To £700/Week) Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Phone Interviews. With most of our paid focus group studies, you have the option to participate remotely online or in-person. This is a great way to earn additional income from the comfort of your home. We need participants on the following topics: • Child Related (individuals with children 18 yrs or younger), • Cell Phones (Apple, Android, or Windows...Prepaid or Contract), • Entertainment (TV shows, movies, and video games), • Food (If you buy fast food, casual dining, or upscale dining), • Sports (Casual viewers and die-hard fans), • Electronics (Tell us which devices you prefer and why), • Pets (Animal lovers needed! Dogs, cats, and other pets), • Automobiles (Do you own, make payments, or lease your vehicle?), • Show up at least 10 minutes prior to discussion start time., • Participate by completing written and oral instructions., • Complete written survey provided for each panel., • MUST actually use products and/or services, if provided. Then be ready to discuss PRIOR to meeting date., • Must have either a smart phone with working camera or webcam on desktop/laptop., • Must have access to a reliable internet connection, • Desire to fully participate in one or several of the above topics, • Ability to read, understand, and follow oral and written instructions., • Data Entry Clerk experience is not necessary, • Flexibility to take part in discussions online or in-person., • No commute needed if you choose to work from home remotely., • No minimum hours. You can do this part-time or full-time, • Enjoy free samples from our sponsors and partners in exchange for your honest feedback of their products., • You get to review and use new products or services before they are launched to the public., • £55-£120 (per 1 hour session), • £250-£700 (multi-session studies) You must apply on our website and complete questionnaire to see if you qualify. This position is perfect for anyone looking for temporary, part-time or full-time work. The hours are flexible and no previous experience is needed. If you are a data entry clerk or someone just looking for a flexible part time remote work at home job, this is a great way to supplement your income.

Step into a UK CSO Technician role where innovation meets precision in clinical trial packaging excellence. Proclinical is seeking a UK_CSO Technician to join a dynamic team in the dermatology and pharmaceutical sector. This role focuses on supporting clinical trial packaging operations, ensuring compliance with quality standards, and contributing to process improvements. You will work both independently and collaboratively to maintain high standards in a GMP-regulated environment. Responsibilities: Execute cleaning, start-up, and completion of clinical trial packaging operations following Standard Operating Procedures. Perform primary packaging tasks, including bottle filling of oral dosage forms using various equipment. Conduct labelling and assembly of clinical trial supplies, utilizing automated labelling and walleting equipment. Monitor and control production processes and equipment, troubleshoot issues, and escalate problems as needed. Develop and apply knowledge of electronic systems, such as SAP, to support operations. Complete electronic batch documentation, equipment logbooks, and other relevant production records. Adhere to GMP requirements and defined procedures to maintain quality standards in the packaging environment. Work safely, understanding personal responsibility for Health, Safety, and Environmental principles, including risk management and COSHH compliance. Participate in internal audits and contribute to continuous process improvement initiatives. Key Skills and Requirements: Educational background at A-level standard, preferably in sciences or IT-related subjects. Strong problem-solving skills and the ability to collaborate effectively with colleagues. Excellent communication and interpersonal skills. High attention to detail and ability to meet deadlines accurately. Proficiency in computer systems and willingness to develop and share knowledge. Experience in a GMP-regulated packaging and labelling environment, ideally within clinical trials. Working knowledge of SAP and basic understanding of clinical trial operations. If you are having difficulty in applying or if you have any questions, please contact Dean Fisher at (url removed). Apply Now: If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data

Registered Manager (Nursing) | Merseyside / Liverpool | c.£70,000 + £10k Bonus The hard part's done. Now someone gets to build on it. Plenty of management roles ask you to dig a home out of a hole. This one's different. A family-owned care group is looking for a Registered Manager to take the helm of one of its Liverpool nursing homes, a home that's been quietly moving in the right direction and now needs a leader to keep that momentum going and push for more. If you've spent your career inheriting other people's problems, this is the change of pace worth a phone call. You'd be steering an established team that knows what good looks like, with the freedom to lead and the backing of a group that puts its money where its values are: training, technology, and homes people are proud to work in. It's a clinical leadership role with commercial teeth. You set the standard, you own the outcomes, and you're trusted to get on with it. The non-negotiables: Valid NMC pin (RGN or RMN) Management or strong deputy experience in a nursing home A track record of holding standards and lifting a team with you Someone who leads from the floor, not the office chairWhat's in it for you: Circa £70,000 package A home with positive momentum to build on, not rebuild from scratch Genuine autonomy with proper head-office support behind you A long-term, family-owned employer that reinvests in its peopleIf that sounds like your next move, send your CV (don't worry if it's not up to date) or call for a confidential, no-strings conversation. Complete discretion as standard. Recruitment Panda Ltd is acting as an Employment Agency in relation to this vacancy. We are committed to equal opportunities and welcome applications from all suitably qualified candidates regardless of race, sex, disability, religion, sexual orientation, or age. By submitting your application, you consent to Recruitment Panda Ltd processing your personal data in accordance with our Privacy Policy, a copy of which is available on request (or via the below link where this is viewed on (url removed))

This role involves supporting the Clinical Trials Unit and providing statistical advice on clinical research studies. The Royal Marsden NHS Foundation Trust is seeking a Senior Statistician/Statistician to join the Research Data & Statistics Unit.

The Senior Manager, Clinical Data Management provides oversight of lead Data Manager(s) on assigned clinical data management projects in multiple therapeutic areas to assure proper planning and execution for data management results that meet Regeneron standards and within timelines. Supervises DM di

United States Digital Space LLC is seeking a SAS Programmer to join their Clinical Database Programming & Biostatistics department based in London, UK. This role requires attention to detail and a strong programming background to produce key analysis datasets.

Stars Arena in London is looking for an experienced Data Architect specialized in Clinical Knowledge Graph. Ideal candidates should be adept in graph databases and data analysis. The role involves designing, developing, and maintaining scalable data pipelines using SPARQL and Python, as well as opti

This role requires a senior-level expert to ensure the quality of clinical data for AI systems. As a fully remote position, you will design clinical trial protocols, interpret data for regulatory submission, and evaluate AI analyses to maintain high standards. Alignerr is seeking a Principal Clinica

This role involves providing expert consultation on neurological cases, enhancing AI models, and maintaining high-quality clinical documentation.

Experience working with real‑world health or clinical datasets (e. Experience working in or alongside CROs, digital CROs, clinical research organisations, or clinical technology companies is desirable. Significant experience applying data science or advanced analytics within health, life sciences,

Lead exploratory data analysis on complex time-series datasets generated from clinical trials, internal studies, and external research databases. Collaborate with domain experts to translate clinical and physiological requirements into robust data analysis workflows. As a Senior Clinical Data Scient

Oversee data management strategy and execution, including database design, build, maintenance, and database lock activities, in alignment with biostatistics. The Vice President of Clinical Operations and Data Management (CODM) provides strategic leadership for the planning, execution, and oversight

University Hospitals of Leicester NHS Trust is looking for an Archivist and Data Admin to ensure high-quality patient care within clinical research settings. With a focus on patient confidentiality and ethical conduct, this role is crucial to the success of clinical research initiatives.

Our Future Health UK is seeking a detail-oriented Senior Scientist to transform healthcare by leveraging extensive health data. You will support scientific feasibility assessments for clinical research studies and collaborate with diverse teams to evaluate recruitment strategies.

The successful candidate will work collaboratively with various clinical teams, manage their own studies, and contribute to the efficient running of clinical trials. The role involves monitoring research participants, handling clinical trial documentation, and ensuring compliance with ICH Good Clini

MMS Holdings Inc is seeking a Senior Biostatistician to contribute to clinical study protocols and statistical analysis plans. Responsibilities include advanced statistical evaluation, dataset quality control, and collaboration with programming teams. Strong proficiency in SAS and a sound understand

Data Architect - Clinical Knowledge Graph. Design, develop, and maintain scalable data pipelines using SPARQL and. Create and optimize complex SPARQL queries to retrieve and analyze data.

Alnylam Switzerland GmbH is seeking a Senior Manager, Clinical Data Management to lead data management activities for clinical studies. Applicants should have at least 10 years of experience in the biotechnology field, with expertise in managing global studies, excellent organizational skills, and f