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Registered Veterinary Nurse – Hospital Up to £36,000 DOE + attractive benefits package Full time or part time applications South Leeds Are you a qualified RVN wanting to support referral services and grow your skillset? Looking for a new role with state-of-the-art equipment and advanced technology? Do you want to work with an experienced and friendly team? A rare opportunity has opened for a RVN to join a hospital on the outskirts of Leeds. This hospital is a comprehensive 24/7 site which provides referral services for about 20 local practices as well as their standard 1st opinion caseload. You have the chance to rotate through all areas of the hospital from wards to theatre, allowing you to build confidence and specialise if you choose to. As a vet nurse here, you would be able to maximise your potential as you can focus on admitting patients, monitoring anaesthetics, recovering, and discharging patients. While also having the opportunity to assist with advanced cases and surgically assist in schedule 3 procedures. If you would like to have exposure to a wide variety of cases, this is the place! The Team: The team consists of over 60 members of staff, including vets and nurses with postgraduate certificates across ECC, Small Animal Surgery, Medicine, Dentistry, and Anaesthesia. Ideally you will feel confident as a nurse and be enthusiastic, cheerful, and have great customer service skills. What’s in it for you? • Competitive salary, • Generous CPD package, • Pension Scheme, • Paid membership fees (RCVS, BVNA, VDS), • Social events and a focus on wellbeing, • Exclusive discounts and rewards Location: The surgery is Iocated in the outskirts of Leeds with excellent transport links to the centre of Leeds, Bradford, Sheffield, Manchester, Huddersfield, Doncaster, and surrounding areas. Want to apply or want more information? Once you submit your CV, someone will be in contact with feedback and an option for an informal chat within 2 working days. Feel free to call Compass Associates mainline and ask for Carina Walker, though information will be limited without a CV. Recommendations Compass Associates Ltd are working in partnership on this position. If you are not interested, but know someone who is, we offer £200 vouchers for each successful recommendation.

Therapy Area: Mental Health and General Medicine We’re looking for a passionate Key Account Manager to join our field team. You’ll connect with healthcare professionals across primary and secondary care — sparking meaningful conversations, driving awareness, and helping make a real difference to patients. What You’ll Do • Build strong relationships with HCPs across your territory., • Drive engagement using a mix of digital tools, CRM, and face-to-face interactions., • Maximise prescribing opportunities by guiding customers on the patient journey., • Keep admin and reporting slick so you can focus on what you do best — engaging people., • Collaborate closely with your team to make this launch a success. What We’re Looking For • 3+ years’ experience in healthcare/pharma engagement or primary care., • Confident using multi-channel platforms and CRM systems., • Excellent communicator with strong influencing skills., • Familiarity with the NHS landscape., • Degree (or equivalent) and ABPI certification are a bonus., • Full UK driving license. Why You’ll Love It • A supportive, upbeat team that loves to celebrate success., • Competitive package with performance-related rewards. Ready to engage and inspire? Click the easy apply button or get in touch with Sarah Whitby on 01225 336 335 to hear more information!

Job Title: Pharmacist Industry: Pharmacy Location: UK Salary: £45,000 - £60,000 + Package Organisation Overview: A leading independent Pharmacy Group in the UK are looking for a qualified Pharmacist or a newly qualified to support with Pharmacy first and enhance service delivery to the local community. Job Summary: We are looking for a patient-oriented Pharmacist passionate about increasing the quality and quantity of service delivery in the local community. The successful candidate could be a current IP or Pharmacist looking to pursue the IP qualification which is fully supported by our client. Tier 2 applications are supported. Job Responsibilities: • Advising Customers on health concerns, • Dispensing medication, • Enhancing service quality, • Performing health advocacy, • Knowledge of medicine and pharmacology, • Customer service, • Good communication and active listening, • Leadership and management, • Organisation and time management, • Emotional resilience, • Teamwork and interpersonal skills, • Problem-solving and analytical skills, • Adaptability and flexibility Job Qualifications: · GPHC Qualification or equivalent

Emergency Medicine | General Medicine | Accredited & Non-Accredited Roles PLEASE NOTE: ONSITE ROLES Imagine spending a year in one of the most beautiful parts of the world — where your medical career grows as fast as your tan. We’re inviting junior doctors, registrars, and clinical fellows from the UK and Ireland to experience life and work in NSW, Australia. These 12-month hospital contracts offer a rare chance to combine professional development with a true Australian adventure — from bustling coastal cities to welcoming regional and rural communities. Now is the perfect time to apply for the February 2026 intake, with opportunities also available for those preferring a mid-year (August 2026) start. What’s on offer: • 12-month fixed-term contracts across NSW — city, regional, and rural hospitals, • Accredited and non-accredited positions available, • Roles in Emergency Medicine and General Medicine, • Salaries as per NSW Health state award, • Relocation and accommodation assistance packages, • Tailored matching to your preferred role and lifestyle, • Full registration and visa support from our in-house Regulatory & Migration team, • Seamless onboarding and ongoing support throughout your stay Eligibility: You must be eligible for registration via the Competent Authority Pathway (UK or Ireland medical qualification). Why Sydney? Picture a harbour city where world-class hospitals meet world-famous beaches. Sydney blends cutting-edge medical practice with a vibrant, multicultural lifestyle — from coastal walks and café culture to iconic arts and dining. It’s a place where your career can thrive while you enjoy one of the most liveable cities on earth. Why New South Wales? From the rugged beauty of the Snowy Mountains to relaxed coastal towns and dynamic regional centres, New South Wales offers remarkable diversity in both lifestyle and practice. Whether you’re drawn to major tertiary hospitals, thriving regional hubs, or coastal communities, NSW combines professional opportunity with an unbeatable quality of life. Apply now to secure your place for the 2026 intake and start planning your Australian medical adventure. (Wavelength International — trusted medical recruitment specialists connecting doctors with life-changing opportunities since 1999.)

Consultant in IVF Location: London, Manchester, Birmingham, Kent, Nottingham, Oxford Contract: Permanent | Full-time Are you an experienced IVF Consultant looking to take the next step in your career? Our client, a large national IVF provider is looking for IVF Consultants to join their team in the above locations. What You’ll Do: • Provide clinical services in the field of reproductive medicine as part of a multidisciplinary team. You will be responsible for ensuring that the highest standards of clinical care are delivered in line with company objectives as well as national standards., • You will work closely with the Medical Director, the medical community of the organisation and the wider multidisciplinary team to provide standardised practice across the organisation in addition to continually striving to improve and develop services further. They will be expected to actively participate in clinical governance and quality management of the local service., • The post-holder will work with the Medical Director and colleagues in the management of the rota to ensure activity is achieved and consistent safe cover is available., • You will carry out your roles in a way that supports and delivers through our shared values of compassion, collaboration, and expertise. What We’re Looking For: • Experienced Consultant/Associate Specialist who has worked in the UK., • MRCOG., • In-depth demonstratable experience in IVF with successful outcomes. Why Join? You’ll be part of a pioneering team in fertility care with access to cutting-edge treatments, continuous professional development, and the opportunity to transform lives truly. Benefits: • 33 Days annual leave (inc. 8 public holidays), • Clinical development framework, • Level 3, 5 and 7 leadership apprenticeships, • Research opportunities To register your interest in this role or to find out more, don't hesitate to get in touch with Chris Hemming: 0203 910 0570

Precision for Medicine is hiring a Medical Director/Senior Medical Director – Oncology to join our global team! candidates can work remotely in any of the following locations: UK, Poland, Hungary, Romania, Serbia or Slovakia. Position Summary The Medical Director serves as the project physician and provides medical and scientific expertise to project teams. The Medical Director’s primary focus of work will be to ensure the accuracy and integrity of the data resulting from the trial, with concentrated focus on patient safety. This position also participates in the strategic planning and execution of critical development programs for a variety of clients in Oncology/Haematology contributes to the development of Precision’s Medical team and supports Business Development activities. Essential functions of the job include but are not limited to: • Work closely with senior leaders in Medical, Operational Strategy, and Business Development to support client engagement., • Support Business Development and Proposals teams by participating in the RFP process; prepare medical considerations section for proposals; and support or participate in bid defense meetings., • Write or edit scientific content of deliverables within budget and timelines., • Collaborates with Regulatory Affairs on regulatory product landscape and strategies as a part of overall drug development strategy., • Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts)., • Review and revise protocols, case report forms, training materials, project specific tools, analysis plans, study designs, clinical trial reports and new drug applications., • Review laboratory values, adverse events, coded adverse event and medication data, and data tables, listings and figures as needed., • Serve as a medical resource for study sites, the project team and clients., • Assist in the preparation of the Medical Monitoring Plan and materials for investigator meetings and staff training sessions., • Assume responsibility for medical and safety monitoring on assigned projects., • Participate in feasibility discussions relating to specific project proposals., • Develop training modules and provide training concentrating on disease states., • Participate in process improvement activities., • Collaborate with Vice President, Global Medical and other members of the Medical Science Department to support growth and development activities globally. Qualifications Minimum Required: • MD, DO, MBBS, or equivalent medical qualifications., • 5+ years of Oncology clinical experience., • Ability to strategically analyze oncology clinical trial protocols., • Availability for domestic and international travel including overnight stays (approximate 30% travel requirement). Preferred • Experience working as a Medical Director for a CRO or Pharmaceutical company., • Oncology Fellowship or equivalent., • Maintains current scientific and medical knowledge base. Skills/Competencies • Ability to deliver on commitments; understands the service culture., • Strategic thinker who can build strategic drug development solutions associated with novel development programs, study designs, and patient populations., • Demonstrates a high degree of professionalism, as evidenced by punctuality, positive interactions with customers and teammates, including good interpersonal skills., • Communicate effectively in the English language both verbally and in a written form., • Conduct formal presentations to a wide variety of audiences including colleagues., • Strong visual and presentation skills., • Ability to work effectively in a fast-pacing team setting, with minimal supervision., • Proven efficiency in working remotely. Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. Any data provided as a part of this application will be stored in accordance with our ___ For CA applicants, please also refer to our ___. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at . It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Company Overview SiPhox Health is redefining how people access and act on their health data. By combining at-home blood testing with advanced AI interpretation, we deliver clinical-grade insights that empower individuals to take control of their health. Our mission is to enable personalized, preventative care that's data-driven, accessible, and actionable. Position Summary We're hiring an Endocrinologist to serve as a Thyroid Product Advisor for our new thyroid health program. In this role, you'll provide clinical expertise to shape our thyroid testing offerings, guide content development, and ensure our thyroid-related insights and recommendations meet the highest medical standards. You'll be instrumental in building a best-in-class thyroid health solution—from biomarker selection and interpretation protocols to educational content and clinical workflows. This is an opportunity to translate your endocrinology expertise into a scalable platform that helps thousands understand and optimize their thyroid health. Position Details • Employment Type: Independent Contractor / Consultant, • Schedule: Flexible, approximately 5-10 hours per week with potential to scale, • Location: Fully remote (worldwide candidates welcome), • Time: Flexible within US business hours (8 AM - 6 PM ET preferred for team collaboration) Key Responsibilities • Clinical Protocol Development: Define which thyroid biomarkers to test, optimal testing protocols, and interpretation frameworks for various thyroid conditions, • Content & Education: Review and refine AI-generated insights, create educational materials, and develop guidance for thyroid-related recommendations, • Product Strategy: Advise on product features, user experience, and clinical workflows specific to thyroid health assessment and monitoring, • Quality Assurance: Review flagged cases, validate interpretation algorithms, and ensure clinical accuracy across the thyroid program, • Team Collaboration: Work closely with our product, data science, and clinical teams to integrate endocrinology best practices into our platform, • Research Integration: Stay current with thyroid research and help incorporate emerging evidence into our testing and interpretation approach, • Case Consultation: Provide expert guidance on complex or edge cases that require specialized endocrinology knowledge Required Qualifications Must-have: • MD or DO with board certification (or equivalent) in Endocrinology, • Active medical license in good standing, • Strong clinical background in thyroid disorders (hypothyroidism, hyperthyroidism, Hashimoto's, Graves', thyroid nodules, etc.), • Experience interpreting thyroid function tests (TSH, Free T3, Free T4, thyroid antibodies, etc.), • Excellent written and verbal English communication skills, • Ability to translate complex endocrinology concepts for non-specialist audiences, • Experience in preventive or functional medicine approaches to thyroid health, • Background in digital health, health tech, or telemedicine, • Familiarity with AI/ML applications in healthcare, • Experience developing clinical protocols or guidelines, • Interest in personalized medicine and health optimization beyond disease management, • Reliable internet connection, • Proficiency with video conferencing and collaborative tools (Slack, Google Workspace, etc.), • Available for occasional synchronous meetings during US business hours What We Offer • Remote, flexible consulting arrangement, • Competitive compensation commensurate with experience, • Opportunity to shape a novel thyroid health platform from the ground up, • Direct impact on how thousands of people understand and manage their thyroid health, • Collaboration with a mission-driven team at the intersection of medicine, AI, and consumer health Ideal Candidate Profile You are an endocrinologist who is passionate about making thyroid health more accessible and understandable. You're excited about the potential of at-home testing and AI to democratize access to quality thyroid care. You have strong clinical judgment but also appreciate the value of empowering patients with knowledge and actionable insights. You're comfortable in a startup environment where you'll help build something new rather than follow established playbooks. Application Process Please submit your CV along with a brief introduction covering: • Your endocrinology background and areas of clinical focus, • Experience with thyroid disorders and biomarker interpretation, • Your interest in digital health and personalized medicine, • Availability and preferred weekly time commitment

Director Biostatistics | Global Pharma | UK | Home Based | Global Pharma recognised for its commitment to innovation and patient impact, is expanding rapidly in the UK. As part of this growth, the company is offering a rare opportunity for a Director Biostatistics to join them. This is an organisation where excellence is not just expected, it’s cultivated. Known for its open, forward-thinking culture and genuine commitment to purpose-driven science, the company provides an environment that inspires, supports, and rewards. Every contribution here matters. Every voice is valued. And every project pushes the boundaries of what’s possible in modern medicine. As a Director Biostatistics you will be joining a cross-functional team that requires strong independent leadership to support clinical and observational studies, medical affairs strategies, biomarker and PK/PD analyses, or regional projects. The Director may also lead statistical efforts for early-stage assets or serve as a methodology expert, ensuring high-quality data analysis and interpretation across a variety of programs. What you will be doing: • Lead statistical strategy for haematology oncology, serving as compound-level statistical lead across development, evidence generation, and regulatory/payer interactions., • Develop integrated statistical strategies across trial phases (early, pivotal, RWE, post-marketing), aligned with product profile and development goals., • Provide cross-functional leadership across clinical, medical affairs, RWE, safety, and biomarker statistics., • Represent the organisation in global regulatory and payer discussions (FDA, EMA, PMDA, HTA), guiding statistical input for submissions and evidence packages., • Act as an individual contributor (no line management) while mentoring study-level statisticians., • Present findings clearly to stakeholders and leadership., • Ensure integrated data availability for submissions and marketing support., • Contribute to due diligence, data review, and expert statistical guidance., • Implement and oversee advanced statistical methods. What you will need: • PhD or Master’s in Biostatistics, Statistics, or related field., • Significant oncology clinical development experience, including regulatory submissions and statistical strategy leadership., • Expertise across trial design, biomarkers, exploratory analytics, RWE, safety, and post-marketing support., • Experience with Bayesian methods, adaptive designs, external control arms, and AI/ML in clinical development., • Knowledge of real-world data sources, integration, and interpretation., • Recognised scientific contributions (publications, presentations, or working groups such as ASCO/ESMO)., • Strong leadership presence in external regulatory/HTA/scientific discussions., • Proficiency in SAS (R preferred), with solid understanding of data management and programming practices., • Experience in international teams and ability to communicate complex methods clearly. What to do next: If this opportunity is of interest, please apply now with your CV or reach out to arrange a confidential discussion about other potential opportunities

Lead Physician – London Overview An exciting opportunity is available for a senior medical professional to take a leadership role in the delivery of clinical trials involving various Therapy area's. The position is ideal for someone with prior Principal Investigator experience and a strong interest in mental health innovation. You’ll be working across dynamic, multi-disciplinary teams, guiding trials from early phases through to completion, while maintaining the highest standards in clinical care, compliance, and operational delivery. Role Focus The successful candidate will be responsible for safeguarding participant wellbeing, ensuring trial integrity, and upholding compliance with all relevant clinical regulations and best practices. In this role, you’ll help shape the future of research in an evolving area of mental health treatment. Key Duties and Responsibilities • Take full responsibility for the medical conduct of clinical studies as the lead investigator, • Ensure all research activities comply with Good Clinical Practice (GCP) guidelines and regulatory standards, • Conduct eligibility assessments, safety evaluations, and clinical reviews throughout the study lifecycle, • Make appropriate clinical decisions regarding patient inclusion, dosing readiness, and follow-up care, • Supervise the reporting of any adverse or serious adverse events and ensure timely communication with relevant oversight bodies, • Mentor and support clinical teams involved in research delivery, providing ongoing guidance and medical input, • Collaborate effectively with operational teams, sponsors, and external research partners, • Review and sign off on essential clinical documentation, including source notes and trial case report forms, • Oversee the use, control, and accountability of investigational products and other study-related medications, • Monitor the collection and quality of structured clinical assessments and psychiatric rating scales, • Keep up to date with developments in psychedelic research and relevant clinical guidelines Skills and Experience Required • Medical qualification with active professional registration and licence to practise, • Specialist accreditation or membership (e.g., psychiatry, internal medicine, or similar), • Prior experience acting as Principal Investigator on clinical trials, • Solid understanding of regulatory frameworks including GCP, FDA, EMA, and other global standards, • Previous involvement in psychiatric or CNS-focused studies preferred, • Confident in managing clinical risk and making sound medical decisions, • Proficient in clinical assessments and familiar with tools such as MINI, CAPS-5, or C-SSRS, • Strong communicator, capable of working with diverse teams and external stakeholders, • Comfortable with oversight of investigational products and protocol compliance

Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out ___ What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. The Medical Affairs content teams create and review scientific content for a variety of deliverable types such as slide decks, eModules, infographics, videos, medical information responses, and publications. The team leverages the clinical and scientific knowledge and applies this knowledge to our clients’ business problems to reach to various target audiences such as medical affairs teams, sales reps, physicians, nurses, and patients across different therapy areas. In light of this, the role holder in Content Solutions would get an opportunity to learn and partner with healthcare clients on various projects. The Job entails the following but not limited to: • Subject matter expertise with specific therapeutic areas/disease states in order to partner and collaborate with Clinical Research Physicians and Scientists to develop medical content that is aligned with the brand strategy and medical communications plan. Strong understanding of the Medical Affairs tactic types which includes but not limited to manuscript slide sets, competitive intelligence slide sets, MSL slide decks, disease state education decks, standard response questionnaires, CFAQ documents to answer HCP questions, and Educational Materials etc., • Local adaptation of global scientific contents in local language and according to the local regulations and PI, • Interpret and analyze complex data, research findings and scientific information to create clear, concise, and accurate tactics for different audiences and channel, • Attend the kick-off call with advance preparedness to understand the scope of work. Communicate the minutes of the meeting and timelines clearly to the Project Owners. When needed, provide explicit guidance and set clear expectations for the editors, graphic designers, PMC, and MCA team. Address their comments and concerns promptly to ensure smooth progress of the project, • Ensure the delivery of quality content with appropriate reference citations and style guide alignment, • Effectively prioritize tasks while managing multiple projects and proactively communicate any changes or expectations to all stakeholders. Maintain familiarity with the tools, software, and processes utilized throughout the project lifecycle, • Be open-minded and adaptable to changes in tools, software, and processes. Adjust writing practices in response to new guidelines, research findings, or feedback, and remain flexible in managing evolving project requirements. Skillset: • Minimum 7 to 12 years of medical/scientific writing experience in pharmaceutical companies or medical communications agencies, • Understanding of any specialty area of medicine (preferred) or an overall understanding of the medical field., • Strong flair and passion for creating and reviewing medical communications. Strong written and verbal communication/presentation skills., • Passion for networking., • Strategic and creative mindset, • Partnering with Clinical Research Physicians and Scientists and MSLs, • Project management, • Being up-to-date with the latest technical/scientific developments and relating them to various projects., • Well versed with MS office suite, GraphPad Prism, VeevaVault MedComms and AEM, • Basic knowledge of statistical analysis and data interpretation Education: M. Pharm/ Pharm. D/ BDS / MDS/Ph.D./ Any life science graduate with publication or medical writing and reviewing experience Language Proficiency: English (Writing and Spoken Proficiency) EQUAL OPPORTUNITY: Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

Interim Chief Medical Officer – Healthcare Organisation, East of England – Start ASAP – circa 4-6 Months – Band VSM We are currently working with our client, a healthcare organisation based in the East of England, who are looking for a new Interim Chief Medical Officer. This role is looking to start ASAP and will be for circa 4-6 months. The Interim Chief Medical Officer job will ideally be performed on a 4-day week basis. Regarding remuneration, this role falls inside IR35 and is band VSM, via a Fixed Term Contract. In addition, the successful candidate will need to have some weekly on-site presence. Reporting to the Chief Executive, the role encompasses the following core duties: • Providing strategic medical leadership and clinical guidance to the Board, • Leading the development and continuous improvement of clinical quality, workforce capability, and governance, • Building strong and collaborative relationships with relevant ICBs, professional bodies, and regulators Candidate Profile: The organisation is seeking someone with a GP or Emergency Medicine background, and with strong experience on the provider side rather than commissioning. How to Apply – If you would like to apply for this position, please submit an up-to-date copy of your CV that supports the criteria set out in the person specification as well as your contact details, availability, and desired rate. Due to the number of applications, we are currently receiving for roles, we will only be in contact with candidates who meet the required criteria to discuss the role further.

Epidemiologist 12m, remote/hybrid Key responsibilities: • Improve disease understanding relevant to drug development: incidence, prevalence, risk factors, natural history course, treatment patterns, comorbidities, co-medications, outcome measures, phenotypes, biomarkers, unmet needs, and their variations across domains such as demographics and geographies., • Support clinical trial design, in particular identification of the target population, protocol development, patient recruitment and patient medical history data ascertainment., • Contribute to medication safety evaluation: provide background event rates, synthesize existing evidence including through meta-analyses, identify high-risk populations., • Support post-marketing surveillance activities: risk evaluation mitigation strategies, epidemiology studies for signal detection and inference, post-authorization studies of treatment benefit and risk., • Critically appraise existing epidemiology evidence and create new evidence through delivery of specific research plans/protocols and analysis of healthcare databases available within. Experience required: • 5 years or more in Epidemiology in the pharmaceutical industry or equivalent experience in an academic or government setting., • Significant experience applying epidemiologic methods to study a variety of questions in support of medicine development (safety, effectiveness, natural history of disease), • Demonstrable experience leading pharmaco-epidemiologic research programs in a drug development environment and use of real world data (EMR or claims), • Excellent oral and written communication skills and demonstrated ability to communicate scientific evidence to peers and at scientific meetings., • PhD required in epidemiology or a relevant discipline (i.e. health services research, health outcomes research, public health, statistics or pharmaceutical sciences)

3D Digital Treatment Designer We require you to possess a strong sense of curiosity and a willingness to learn. The company looks forward to growing together with you. Job Responsibilities: 1. Responsible for designing 3D treatments using Smartee's Smart check design software., 2. Support customer by phone, email and/or remote support., 3. Active collaboration with sales and customer service group to fully meet customer needs. Job Requirements: 1. Bachelor's Degree above or equivalent experience /certifications., 2. Excellent computer literacy., 3. No limit to majors, but Medical/Dental Medicine majors is preferred., 4. Holding a PSW visa., 5. IELTS score of 6.5 or above., 6. Chinese and English can be used as working languages. We Offer 1. Systematic training and long-term learning time., 2. Competitive salary and benefits., 3. Opportunities for career growth and professional development., 4. A collaborative and supportive team environment.

Are you passionate about using your ophthalmology knowledge and skills to help others? Answer your calling, and take your leave of purpose. The Tshemba Foundation is appealing to South African ophthalmologists to fill a critical health care gap in rural South Africa’s Mpumalanga and Limpopo provinces where shortages are posing substantial challenges to adequate eye care. Tshemba's efforts to improve vision initially focused on cataract surgery, however, screenings in the community and clinics have indicated an urgent need for non-surgical interventions and ophthalmological services. To take action against blindness prevention, alongside our partners, we’ve expanded our cataract services to include non-surgical interventions in diagnostics and treatment. In your role as a volunteer ophthalmologist you will: • screen and care for diabetic retinopathy, glaucoma and keratoconjunctivitis, • perform cataract operations over extended weekends at our cataract camps, • provide postgraduate support to medical staff in training, • engage in skills development and/or formal teaching for local staff about eye pathology Requirements: • A current medical license in good standing, • Registration with the Health Professionals Council of South Africa (HPCSA), which we assist international volunteers to obtain. Tshemba offers its volunteers free, safe and secure accommodation at its Volunteer Lodge, situated in Moditlo Private Game Reserve. The Lodge serves as a welcome off-duty refuge where like-minded healthcare providers relax after an intense day of work. Here they exchange ideas, create healthcare solutions for daily challenges faced and connect with peers from all over the world, all the while taking in the magnificent natural surroundings. It is important to recognize that while you will be making a massive contribution to eye care in an impoverished rural area, you will have down time. We see this as a win-win with time for you to pause, think and to recharge your batteries. Health professionals who have volunteered with Tshemba tell us that they have been re-energized and transformed by the experience, and their passion for medicine reignited. Please reach out if you have any questions and to discuss volunteering your time.

Consultant Opportunities at Wye Valley NHS Trust – County Hospital, Hereford We are currently recruiting for several consultant positions across the following specialties: Consultant Stroke ×3 Consultant General Internal Medicine (GIM) ×3 Consultant Haematology ×2 Consultant Histopathology ×1 Consultant Community Paediatrics ×1 Consultant Gastroenterology ×1 Consultant Neurology ×1 These roles can be offered on a permanent or fixed-term basis (minumum 12 months), with full job descriptions available once applied If this opportunity isn’t for you but you know a Consultant who may be interested—or a friend or colleague within six months of joining the Specialist Register via the CCT or CESR pathway please get in touch as we offer a £1,000 referral bonus for each new doctor who joins our system and remains in post for 13 weeks. For more details or to apply, please get in touch today!

We are supporting an innovative Bio-MedTech company operating at the intersection of advanced therapies, biologics, wellness, and digital health and they are now hiring a VP of Regulatory Affairs. The role will be required to shape the global regulatory strategy for a fast-growing Bio-MedTech expanding across the UK, EU/Switzerland, US, Middle East and Asia. The role is ideal for a senior regulatory leader who thrives in a pioneering, fast-moving environment and wants to be part of a mission pushing the boundaries of human health and longevity. Key Responsibilities: • Own and define the global regulatory roadmap across multiple jurisdictions, • Clarify classifications and compliant claims for novel biologics, ATMPs, wellness interventions and digital innovations, • Lead early scientific dialogue with regulators (MHRA, EMA, Swissmedic, FDA and others), • Build the internal regulatory frameworks, quality structures and documentation standards, • Guide communications, partnerships, and clinical/wellness deployments to remain compliant Qualifications: • UK-based senior regulatory leader, • Background in biologics, ATMPs, regenerative medicine, advanced wellness, or novel health technologies, • Experience working on boundaries between medical, biological and wellness classifications, • A strong track record leading regulatory strategy, innovation pathways, or early regulatory dialogue, • Someone pragmatic, solutions-focused, and comfortable building from scratch in a dynamic environment If your interested, or know someone who might be, reach out to me at:

Job Title: Contract Qualified Person Job type: Contract (1 day every 7 weeks with a view to potentially increasing in the future) Salary: £1000 - 1400 per day Location: Remote SRG is working with a global leader in radio-medicine focused on improving clinical outcomes for millions of patients suffering from lung-related conditions. We are looking for a contract QP who will be responsible for the commercial release of radioactive compounds for medicines in the UK. The QP will need to be on the MS license and this is a going to be a generally remote role with a requirement to visit the site once a year. Requirements • Qualified Person capable of releasing commercial products to the UK, • Ideally experienced on radiopharmaceuticals but not required. SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It’s this combination that makes us different. We’re committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

The Training Programme Director will work and support the Head of School in leading the delivery of a wide range of functions, aligned to the NHS England mandate. Ensuring high standards of education and training as defined by the General Medical Council and other national bodies with respect to tra

The post will be available on the basis of a secondment arrangement to NHS England remunerated In line with TPD sessional payments ( – 0. The role of Training Programme Director is to work and support the Head of School in leading the delivery of a wide range of functions, aligned to the NHS Engla

A prestigious educational institution is looking for a Head of Strategic Communications to lead their approach to integrated communications within health and care research. This role involves developing key elements of the communications strategy, working with a variety of stakeholders, and requires

As Head of Strategic Communications, you will lead NIHR’s evolving approach to integrated and powerful strategic communications – critical to the new NIHR Communications Strategy. You will be responsible for leading key elements of the NIHR Communications Strategy, including overall NIHR communi

As a Locum Consultant in Emergency Medicine, you’ll play a vital role in delivering high-quality clinical care in both adult and paediatric emergency medicine. Triple West Medical are seeking a Locum Consultant in Emergency Medicine for our NHS Client based in Essex for 12 months on a salaried Fix

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Precision for Medicine is hiring a Medical Director/Senior Medical Director – Oncology to join our glo

We are working with a fantastic team of Vets, Vet Nurses and a wider Vet practice team who are looking for a Small Animal Vet to lead the practice in the specific area of imaging with a keen interest in medicine where your expertise will be a valuable addition where you will benefit from being looke

Triple West Medical are seeking a Locum Consultant in Emergency Medicine for our NHS Client based in Essex for 12 months on a salaried Fixed Term Contract. Based at the main Hospital, the Emergency Department manages around 450 attendances per day, supported by 16 consultant posts, 25 senior grades,

Join a progressiveteam of clinical and none clinical professionals inMilton Keynesas anA&E Consultant,offering a competitive salary of£100,000to £145,000per annum (negotiable), flexible rota options, and both long-term and short-term contracts.Enjoy relocation support, continuous professional deve

Job ID: VS-280725-01Small Animal Vet Veterinary Medicine Veterinary Imaging Doppler Ultrasound:A superb and true independent veterinary practice with a fantastic local reputation is looking for a Veterinary Surgeon with an interest in Veterinary Medicine as well as Imaging to join this fantastic

Successful candidates will receive second to none one‑on‑one care from one of industry leading specialist Consultant Medicine - Gastroenterology Recruitment Consultants to find the perfect role for you while achieving you the highest possible pay rates. Consultant Medicine - Gastroenterology 120

ST3 Medicine – Cardiology 75 Per Hour– East London. We are seeking to appoint an experienced ST3 Medicine – Cardiology work with our client based in the East London. Successful candidates will receive second to none one-on-one care from one of industry leading specialist ST3 Medicine – Cardi

A leading Medical Aesthetic Clinic in Greater London is seeking a Cosmetic Injector to join their team.In this entry-level role, you will administer anti-wrinkle treatments and dermal fillers while providing outstanding service and results for patients.The position offers valuable training and devel

Join a forward-thinking healthcare provider as a Consultant Medicine Doctor specializing in Acute Medicine.

A healthcare provider in Wakefield is seeking a Family Medicine clinician to provide primary care to an urban underserved population.

On behalf of a great hospital based in the North Midlands, I’m looking for an experienced Cardiology Medicine Locum SPR who could join the friendly department for a minimum of 3 months.

Consultant Medicine – Gastroenterology 120 Per Hour – East Midlands. Consultant Medicine – Gastroenterology – East Midlands. We are seeking to appoint an experienced Consultant Medicine – Gastroenterology to work with our client based in the East Midlands.

A leading healthcare organization in Greater London is looking for a dynamic General Manager to lead the Emergency Medicine department.

Consultant Medicine - Gastroenterology 120 Per Hour – North West England. Consultant Medicine - Gastroenterology. We are seeking to appoint an experienced Consultant Medicine - Gastroenterology to work with our client based in North West England.

Locum Consultant in Rehabilitation Medicine or Neurologist. This is an exciting opportunity to join a dynamic rehabilitation medicine team, working with patients who have complex neurological conditions who require highly specialised holistic rehabilitation care. As part of this team, you will work

Do you want to be a pivotal part of an incredible organisation powering health and care research? Do you have experience of leading transformational strategic communications at a senior level? Are you confident working with senior stakeholders across government, and health and a range of other secto

Our division delivers world‑class care across integrated services, renal and transplant, stroke and neurosciences, acute and specialist medicine, and urgent and emergency care. As Divisional Director, you will provide vision, strategic direction and executive leadership for the Medicine and Integr

We are looking for a motivated nuclear medicine radiologist who will join our fast‑paced, growing radiology department at Blackpool Teaching Hospitals. In early 2021 we refurbished the Central Radiology department to an advanced diagnostic facility, now equipped with 2 nuclear medicine cameras and

A prestigious educational institution is looking for a Head of Strategic Communications to lead their approach to integrated communications within health and care research.This role involves developing key elements of the communications strategy, working with a variety of stakeholders, and requires

A healthcare organization in the South East/Essex region is looking for an experienced Clinical Director & Consultant in Emergency Medicine.

A major UK healthcare provider is seeking a dynamic General Manager to lead the Emergency Medicine department in Greater London.

Ensuring high standards of education and training as defined by the General Medicine Council and other national bodies with respect to training posts and other educational programme in the Yorkshire and the Humber.

A highly accomplished and professional interim manager with a strong NHS vision, enthusiasm and an ability to achieve a successful outcome.Highly experienced in clinician engagement, achievement of National Targets project management and team innovation.Acted as General Manager for Medical Specialti

Divisional Director of Medicine and Integrated Care. Our division delivers world-class care across integrated services, renal and transplant, stroke and neurosciences, acute and specialist medicine, and urgent and emergency care. As Divisional Director, you will provide vision, strategic direction a

Divisional Director of Medicine and Integrated Care. Divisional Director of Medicine and Integrated Care. Our division delivers world-class care across integrated services, renal and transplant, stroke and neurosciences, acute and specialist medicine, and urgent and emergency care.

Registar Medicine – Gastroenterology 75 Per Hour – West Midlands. Grade and Specialty: Registar Medicine – Gastroenterology. We are seeking to appoint an experienced Registar Medicine – Gastroenterology to work with our client based in the West Midlands.