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Care Manager | Boroughbridge, North YorkshireSalary: £35,000 per yearFull-time | Permanent We are recruiting on behalf of Harrogate Neighbours Housing Association for an experienced and confident Care Manager to lead the care team at Heath Lodge in Boroughbridge. This is a hands-on leadership role for someone who is passionate about delivering high standards of person-centred care and building a positive, motivated team culture. The RoleAs Care Manager, you will be responsible for the day-to-day leadership and operational management of care delivery within the home. Key responsibilities include: • Leading, supervising and supporting senior carers, team leaders and care staff, • Promoting a positive environment that upholds dignity, independence and choice, • Ensuring care is delivered in line with individual needs and care plans, • Acting as a visible, hands-on leader, stepping into care delivery where needed, • Conducting team meetings, supervisions and appraisals, • Monitoring performance and implementing support or improvement plans, • Overseeing care documentation to ensure accuracy and compliance, • Supporting safe medication processes and staff competency, • Assisting with rota planning to ensure fair and effective staffing coverage, • Working collaboratively with catering, housekeeping and other departments, • Managing concerns or complaints sensitively and professionally, • Preparing reports for senior management, • Participating in the on-call rota and supporting the team during emergencies About YouWe are looking for an experienced care professional who can combine operational oversight with strong people leadership. Essential requirements:, • Minimum of 5 years' experience within the care sector, • At least 3 years' supervisory experience at Deputy Manager level, • Level 5 qualification in Health & Social Care, • Strong leadership and mentoring capability, • Excellent communication and organisational skills, • A solid understanding of safeguarding, compliance and regulatory standards, • A genuine commitment to delivering high-quality, person-centred care You will be someone who leads by example and creates a culture of accountability, collaboration and compassion. Salary & Benefits, • £35,000 per year, • Ongoing training and professional development, • Free on-site parking, • Paid lunch break with lunch provided, • Group and 1-to-1 wellbeing sessions, • Long service recognition, • Referral bonuses, • Healthcare cash plan, • Blue Light Card with discounts across hundreds of retailers If you are an experienced Deputy Manager ready to step up, or an existing Care Manager seeking a new challenge in a well-established organisation, we would welcome your application. Please apply with your CV outlining your relevant experience and qualifications. Key Appointments UK Ltd will assess your suitability for the role based on the information contained in your CV and application. This includes skills, experience, education, and location. By applying for this role, you give consent for your CV to be processed by Key Appointments for recruitment purposes only. Our full Privacy Policy is available at key-appointments

ABOUT THE ROLE As a Regional Nurse (RGN/RMN) at Barchester, you'll travel across your region to deliver the high clinical standards we're known for. We'll look to you to lead a multi-disciplinary team to make sure that on each shift, at every location, all of our residents get the highest quality care. You can expect a wide range of responsibilities, from making sure new residents are settling in, to helping advance your team members' skills, and developing care plans that are tailored to our residents' physical and mental needs. As a Peripatetic Nurse, you'll have the freedom and autonomy to do things the right way and be truly valued and respected for what you do. ABOUT YOU To join us as a Peripatetic Nurse, you'll need to be a Registered Nurse (RGN/RMN) with a current NMC registration and a teaching, mentoring or supervision qualification. A strong, up-to-date clinical knowledge is important, as is a good understanding of key regulatory frameworks, including the safe administration of medicines, Royal Pharmaceutical guidelines, and NMC standards. We'll also look for a successful track record of producing care plans and detailed risk assessments. Dedicated and ambitious, you'll be able to lead by example your can-do approach and excellent communication skills will motivate the teams in each Barchester care home you work with. REWARDS PACKAGE In return for your dedication, you'll receive a competitive salary plus our sector-leading benefits and rewards package including: NMC registration paid every year Free training and development for all roles Access to wellbeing and support tools A range of retail discounts and savings Nurse Mentor' and Refer a Friend' bonus schemes Offer to pay Health & Care Worker Visa immigration fees (for eligible nurses) And so much more! If you'd like to use your clinical and people skills in an organisation that provides the quality care you'd expect for your loved ones, this is an empowering and rewarding place to be.

Location: York About London Women’s Clinic is a leading private fertility clinic delivering high-quality, evidence-based care in a patient-centred environment. We are seeking a compassionate and experienced Fertility Nurse to join our multidisciplinary clinical team. The role As a Fertility Nurse at LWC, you will manage a clinical caseload and provide safe, high-quality nursing care across the fertility treatment pathway. Working closely with consultants, embryology, nursing, and wider teams, you will ensure care is delivered in line with LWC SOPs and HFEA requirements, while contributing to clinical governance and service improvement. Key responsibilities • Deliver compassionate, patient-centred care throughout fertility investigations and treatment, • Manage a clinical caseload in accordance with SOPs and regulatory standards, • Support safe clinical practice and act as a point of reference for patient care and quality, • Collaborate with multidisciplinary teams to optimise patient pathways, • Support the development of new nursing staff once competent, • Take part in the on-call rota (telephone-based) as required About you Essential: • Registered General Nurse (RGN) with a valid NMC PIN, • Relevant post-registration experience (fertility, women’s health, or acute care desirable), • Strong communication skills with a warm, empathetic approach, • Ability to work autonomously and within a multidisciplinary team, • Commitment to clinical governance and high standards of care Desirable: • Ultrasound scanning experience (preferred but not essential) Benefits • Workplace nursery salary sacrifice scheme, • Electric vehicle salary sacrifice scheme, • Cycle to Work scheme, • Employee Assistance Programme (EAP), • Gym membership discounts, • Staff treatment discounts, • Life assurance, • Pension plan, • Perkbox benefits platform To apply, please submit your CV and a short covering letter outlining your interest in the role. Equality, Diversity & Inclusion: We at London Women's Clinic are an Equal Opportunities employer and recognise the value of a Diverse Organisation. London Women's Clinic appreciates all job applications. If you decide to apply for an opportunity with us, your application will be assessed based purely on your experience, the essential and desirable criteria, and your suitability for the role. Additional Information: • As part of our standard recruitment process this role will require a disclosure and barring service (DBS) check., • We will request two professional references from candidates., • All candidates who progress to the final stages of the recruitment process will be required to provide evidence of their right to work in the UK. This may include but is not limited to passport, VISA or residency documentation.

Research Nurse, full time York £35,000.00-£40,000.00 per year We have an exciting opportunity for a dynamic and motivated Research Nurse to join our brand new site in York! Panthera is an independent Site Management Organisation helping pharmaceutical and contract research organisations find the right patient, for the right trial, at the right time. The Panthera team is run by a world-class team of experts with more than a hundred years of clinical research experience. We put the patient at the heart of everything we do to ensure the best experience and environment for volunteers and participants. Accelerating clinical breakthrough for our customers, our patients, and for future generations. Job Summary The post holder will be responsible for ensuring that nursing activities, related to clinical trials across a wide and diverse range of therapeutic areas, are undertaken following Nursing and Midwifery Council guidelines and as per Good Clinical Practice (ICH-GCP). You will work alongside the wider clinical research team in the assessment and management of patient care pathways. This will involve recruitment, education, monitoring of research participants and the collection and documentation of accurate data. As a skilled communicator, the successful candidate, must also possess excellent interpersonal and problem-solving skills and be able to act as an ambassador for promoting research utilisation and best practice. The normal working hours for the post are Monday to Friday, 8:30am - 4:30pm, although the post holder may need to be flexible to accommodate patient visits and assessments outside of these hours when required. Key Responsibilities • Manage nursing activities relating to clinical trials from the start up on a trial to the close out, working to ICH/GCP guidelines, • Attend site initiation visits (SIV) for any new study and keep up to date with any changes with the study protocols, • Perform PIV patient interest visits (chats) effectively with knowledge and understanding of the study protocol, • Keep patients engaged with the study at each visit to optimize patient retention, • Collecting records, verifying, and entering study data into the source notes, CRF/eCRF and all associated paperwork with a high degree of accuracy, • Promoting and nurturing a welcoming, professional and pleasant environment for staff and participants, • Ensuring that all data queries are acted upon in a timely and efficient manner, • Initiating any emergency reaction when required at site for patients or staff, • Review and regularly check the emergency trolley, • To be able to perform laboratory duties on each study if required, • Always work in compliance of GDPR (General Data Protection Regulation), • To keep up to date with all training, ongoing SOPs/COPs and regulatory standards Ideal Candidate • NMC Registration with no limitations to practice, • 2+ years post registration experience, • Clinical research experience (desirable), • Ability to work in a team within a multidisciplinary environment with minimal supervision, • A patient focused attitude, • Self-motivated and excellent organisational skills There are so many fantastic benefits included when you join Panthera, below are some of those: • An extremely competitive salary, • 25 days holiday a year + bank holidays, • Enhanced Employer Pension Contributions, • Bonus (based part on individual and part based on company performance), • Car leasing scheme - Salary sacrifice scheme for electric car options., • Medicash plan - Reclaim doctor, dentist & optician expenses., • Enhanced Family Policies (Paternity, Maternity, Shared Parental & Adoption Leave). Join us on our journey of building a new kind of organisation. This means we’re opening new ways to work, ground-breaking methods and bringing unexpected teams together Interested? Come and join our journey! Panthera Biopartners is an equal opportunity employer. Panthera will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. Panthera only employs individuals with the right to work in the country where the role is advertised.

Job Title: Clinical Research Nurse Location: York, UK Start Date: ASAP Rate: £175-£225/day Company Overview We are proud to be partnering with a respected and innovative clinical research organisation that is committed to improving patient outcomes through high‑quality clinical trials. Our client delivers a diverse portfolio of studies within a supportive, patient‑centred environment, working to the highest ethical and regulatory standards. This is an exciting opportunity to join a forward‑thinking team that is shaping the future of clinical research. Role Overview Our client is seeking an enthusiastic and dedicated Clinical Research Nurse to support the delivery of clinical trials from study start‑up through to close‑out. This role is ideal for a confident nurse with excellent communication skills who enjoys building rapport with patients and working collaboratively within a multidisciplinary team. You will be instrumental in ensuring protocol compliance, accurate data collection and a positive patient experience throughout the study lifecycle. Key Responsibilities • Oversee clinical trial nursing activities from initiation to close‑out in accordance with ICH/GCP guidelines., • Attend Site Initiation Visits (SIVs) and remain updated on any protocol amendments., • Conduct PIV patient interest visits, providing clear and knowledgeable study information., • Support strong patient engagement and retention throughout each trial., • Collect, verify and accurately record study data in source notes and CRF/eCRF systems., • Foster a safe, professional and welcoming environment for both staff and study participants. Skills & Experience • NMC Registered Nurse with unrestricted practice., • Minimum of 2 years post‑registration experience., • Previous clinical research experience (desirable but not essential)., • Ability to work effectively within a multidisciplinary team with minimal supervision., • Strong patient‑focused approach and excellent communication skills., • Highly organised, self‑motivated and compliant with GDPR and regulatory standards. Interested? Apply now for immediate consideration or contact James Allen on +44 203 868 8607 – We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Planet Pharma is an Employment Business providing Global Staffing services.

Registered Nurse – 3-Month Contract (York & Sheffield) Location: York Contract: 2-3 months Hours: Monday – Friday, 8:30am–4:30pm (on-site) Start Date: ASAP About the Role We are seeking an experienced and dynamic Registered Nurse (NMC Registered) to join a fast-paced clinical research environment, supporting the delivery of high-quality clinical studies across our York and Sheffield sites. This is an excellent opportunity for an adaptable, hands-on professional to contribute to innovative research projects that have a real impact on patient outcomes. You will work closely with multidisciplinary teams to ensure the smooth and compliant running of clinical trials, with a focus on patient safety, data accuracy and operational efficiency. About the Organisation You’ll be joining a rapidly growing, independent clinical research organisation dedicated to improving access to clinical trials for patients and healthcare professionals. With multiple purpose-built sites across the UK, the organisation partners with the NHS, industry sponsors and CROs to deliver high-quality, patient-centred research. Their mission is to make clinical research more efficient, inclusive, and accessible, driving innovation in healthcare. Key Responsibilities • Deliver safe, high-quality nursing care in accordance with Good Clinical Practice (GCP) and regulatory requirements., • Support clinical trials from screening through to follow-up, ensuring accurate data collection and documentation., • Collaborate with investigators, research coordinators and external partners to maintain smooth study operations., • Conduct patient assessments, administer treatments and manage samples as required., • Uphold clinical and ethical standards while maintaining excellent patient care., • Travel between York and Sheffield sites as required (driving license essential). Requirements • NMC registered with no limitations to practice (must be verified before submission)., • Experience in a fast-paced clinical setting (e.g., A&E)., • Previous clinical research experience desirable., • Full UK driving license., • Available for interview via Teams and able to start at short notice.

Clinical Research Nurse Location: York Working Hours: Monday–Friday, 8:30am–4:30pm (on-site) Company: A specialist clinical research organisation operating purpose-built research facilities across the UK. The organisation works in close partnership with pharmaceutical and biotechnology companies to deliver high-quality clinical trials, supporting the development of new and existing therapies. Role Overview We are seeking a dedicated Clinical Research Nurse to support the delivery of clinical trials at our York site. The post holder will manage nursing activities across the full lifecycle of clinical studies, ensuring compliance with regulatory standards and delivering a high-quality experience for study participants. Due to the site location, a full UK driving licence is essential. Key Responsibilities • Manage all nursing-related activities for clinical trials from study start-up through to close-out, in line with ICH/GCP guidelines, • Attend Site Initiation Visits (SIVs) and remain up to date with protocol amendments and study updates, • Conduct Patient Interest Visits (PIVs), demonstrating thorough knowledge of study protocols, • Maintain patient engagement throughout the study to support optimal retention, • Accurately collect, verify, and document study data within source notes, CRFs/eCRFs, and associated documentation, • Create and maintain a welcoming, professional, and supportive environment for both participants and staff, • Ensure data queries are addressed promptly and efficiently, • Respond appropriately to any medical emergencies involving patients or staff, • Regularly review and check the emergency trolley to ensure readiness, • Undertake laboratory-related duties where required by the study, • Work at all times in compliance with GDPR requirements, • NMC registered nurse with no restrictions on practice, • Minimum 2 years post-registration experience, • Previous clinical research experience (desirable but not essential), • Ability to work effectively within a multidisciplinary team with minimal supervision, • Strong patient-focused approach, • Highly self-motivated with excellent organisational and time-management skills

Contract Programme Manager – Product & Pricing Transformation (Insurance) Inside IR35 - Market Rate Duration: 6 months initial with the programme running for 18 months Location: York or London We are seeking an experienced Contract Programme Manager to lead a large-scale Product and Pricing Transformation Programme within a regulated insurance environment. This is a senior delivery role requiring deep experience across insurance underwriting, product design, and pricing transformation. The Role You will be accountable for end-to-end programme delivery, overseeing multiple workstreams spanning underwriting, product, pricing, data, and technology. Working closely with senior stakeholders, you will ensure the programme delivers measurable commercial and operational outcomes while meeting regulatory and governance requirements. Key Responsibilities • Lead and deliver a complex product and pricing transformation programme within an insurance business, • Own programme governance, planning, RAID management, financial tracking, and reporting, • Coordinate cross-functional workstreams including underwriting, product, pricing, actuarial, data, and technology, • Partner with senior leaders to shape delivery strategy, milestones, and benefits realisation, • Manage third-party vendors and system integrators where applicable, • Ensure alignment with regulatory, risk, and compliance expectations, • Drive delivery pace while managing change in a complex, matrixed organisation Essential Experience • Proven experience as a Programme Manager delivering large-scale transformation programmes, • Strong insurance domain expertise, particularly within:, • Underwriting, • Product development, • Pricing / rating / actuarial-led change, • Experience delivering product and pricing transformation initiatives (e.g. target operating models, pricing modernisation, underwriting transformation, platform or rating engine change), • Excellent senior stakeholder management and communication skills, • Strong governance, planning, and delivery discipline in a regulated environment

Trainee Animal Technician We are seeking a motivated and compassionate Trainee Animal Technician to join a close- knit research facility. This is an excellent opportunity for someone looking to begin a long term career in animal technology within a regulated research environment. You will support essential preclinical research programmes by assisting in the care and husbandry of animals, including rodents. Full training will be provided, with structured development toward industry-recognised qualifications. The Role • Provide daily husbandry and welfare monitoring for rodent and aquatic species, • Maintain high standards of cleanliness within animal housing areas, • Prepare feeds, bedding and enrichment materials, • Monitor animal health and behaviour, escalating concerns appropriately, • Accurately complete records in line with regulatory and facility requirements, • Support senior technicians and research teams with routine procedures, • Work in accordance with Home Office regulations and internal compliance standards This role offers hands-on experience within a highly regulated life science setting and provides a clear pathway for career progression within animal technology. About You • A genuine interest in animal care and life sciences, • Strong attention to detail and observational skills, • The ability to follow strict protocols and standard operating procedures, • Good communication and teamwork skills This is an excellent opportunity to begin a career within animal science and contribute to research that supports advancements in medicine and biotechnology.

London Women’s Clinic is a leading private fertility clinic delivering high-quality, evidence-based care in a patient-centred environment. Manage a clinical caseload in accordance with SOPs and regulatory standards. Support safe clinical practice and act as a point of reference for patient care an

Registered Nurse – 3-Month Contract (York & Sheffield) Location: York Contract: 2-3 months Hours: Monday – Friday, 8:30am–4:30pm (on-site) Start Date: ASAP About the Role We are seeking an experienced and dynamic Registered Nurse (NMC Registered) to join a fast-paced clinical research environment, supporting the delivery of high-quality clinical studies across our York and Sheffield sites. This is an excellent opportunity for an adaptable, hands-on professional to contribute to innovative research projects that have a real impact on patient outcomes. You will work closely with multidisciplinary teams to ensure the smooth and compliant running of clinical trials, with a focus on patient safety, data accuracy and operational efficiency. About the Organisation You’ll be joining a rapidly growing, independent clinical research organisation dedicated to improving access to clinical trials for patients and healthcare professionals. With multiple purpose-built sites across the UK, the organisation partners with the NHS, industry sponsors and CROs to deliver high-quality, patient-centred research. Their mission is to make clinical research more efficient, inclusive, and accessible, driving innovation in healthcare. Key Responsibilities • Deliver safe, high-quality nursing care in accordance with Good Clinical Practice (GCP) and regulatory requirements., • Support clinical trials from screening through to follow-up, ensuring accurate data collection and documentation., • Collaborate with investigators, research coordinators and external partners to maintain smooth study operations., • Conduct patient assessments, administer treatments and manage samples as required., • Uphold clinical and ethical standards while maintaining excellent patient care., • Travel between York and Sheffield sites as required (driving license essential). Requirements • NMC registered with no limitations to practice (must be verified before submission)., • Experience in a fast-paced clinical setting (e.g., A&E)., • Previous clinical research experience desirable., • Full UK driving license., • Available for interview via Teams and able to start at short notice.

Clinical Research Nurse Location: York Working Hours: Monday–Friday, 8:30am–4:30pm (on-site) Company: A specialist clinical research organisation operating purpose-built research facilities across the UK. The organisation works in close partnership with pharmaceutical and biotechnology companies to deliver high-quality clinical trials, supporting the development of new and existing therapies. Role Overview We are seeking a dedicated Clinical Research Nurse to support the delivery of clinical trials at our York site. The post holder will manage nursing activities across the full lifecycle of clinical studies, ensuring compliance with regulatory standards and delivering a high-quality experience for study participants. Due to the site location, a full UK driving licence is essential. Key Responsibilities • Manage all nursing-related activities for clinical trials from study start-up through to close-out, in line with ICH/GCP guidelines, • Attend Site Initiation Visits (SIVs) and remain up to date with protocol amendments and study updates, • Conduct Patient Interest Visits (PIVs), demonstrating thorough knowledge of study protocols, • Maintain patient engagement throughout the study to support optimal retention, • Accurately collect, verify, and document study data within source notes, CRFs/eCRFs, and associated documentation, • Create and maintain a welcoming, professional, and supportive environment for both participants and staff, • Ensure data queries are addressed promptly and efficiently, • Respond appropriately to any medical emergencies involving patients or staff, • Regularly review and check the emergency trolley to ensure readiness, • Undertake laboratory-related duties where required by the study, • Work at all times in compliance with GDPR requirements, • NMC registered nurse with no restrictions on practice, • Minimum 2 years post-registration experience, • Previous clinical research experience (desirable but not essential), • Ability to work effectively within a multidisciplinary team with minimal supervision, • Strong patient-focused approach, • Highly self-motivated with excellent organisational and time-management skills

Research Nurse, full time York £35,000.00-£40,000.00 per year We have an exciting opportunity for a dynamic and motivated Research Nurse to join our brand new site in York! Panthera is an independent Site Management Organisation helping pharmaceutical and contract research organisations find the right patient, for the right trial, at the right time. The Panthera team is run by a world-class team of experts with more than a hundred years of clinical research experience. We put the patient at the heart of everything we do to ensure the best experience and environment for volunteers and participants. Accelerating clinical breakthrough for our customers, our patients, and for future generations. Job Summary The post holder will be responsible for ensuring that nursing activities, related to clinical trials across a wide and diverse range of therapeutic areas, are undertaken following Nursing and Midwifery Council guidelines and as per Good Clinical Practice (ICH-GCP). You will work alongside the wider clinical research team in the assessment and management of patient care pathways. This will involve recruitment, education, monitoring of research participants and the collection and documentation of accurate data. As a skilled communicator, the successful candidate, must also possess excellent interpersonal and problem-solving skills and be able to act as an ambassador for promoting research utilisation and best practice. The normal working hours for the post are Monday to Friday, 8:30am - 4:30pm, although the post holder may need to be flexible to accommodate patient visits and assessments outside of these hours when required. Key Responsibilities • Manage nursing activities relating to clinical trials from the start up on a trial to the close out, working to ICH/GCP guidelines, • Attend site initiation visits (SIV) for any new study and keep up to date with any changes with the study protocols, • Perform PIV patient interest visits (chats) effectively with knowledge and understanding of the study protocol, • Keep patients engaged with the study at each visit to optimize patient retention, • Collecting records, verifying, and entering study data into the source notes, CRF/eCRF and all associated paperwork with a high degree of accuracy, • Promoting and nurturing a welcoming, professional and pleasant environment for staff and participants, • Ensuring that all data queries are acted upon in a timely and efficient manner, • Initiating any emergency reaction when required at site for patients or staff, • Review and regularly check the emergency trolley, • To be able to perform laboratory duties on each study if required, • Always work in compliance of GDPR (General Data Protection Regulation), • To keep up to date with all training, ongoing SOPs/COPs and regulatory standards Ideal Candidate • NMC Registration with no limitations to practice, • 2+ years post registration experience, • Clinical research experience (desirable), • Ability to work in a team within a multidisciplinary environment with minimal supervision, • A patient focused attitude, • Self-motivated and excellent organisational skills There are so many fantastic benefits included when you join Panthera, below are some of those: • An extremely competitive salary, • 25 days holiday a year + bank holidays, • Enhanced Employer Pension Contributions, • Bonus (based part on individual and part based on company performance), • Car leasing scheme - Salary sacrifice scheme for electric car options., • Medicash plan - Reclaim doctor, dentist & optician expenses., • Enhanced Family Policies (Paternity, Maternity, Shared Parental & Adoption Leave). Join us on our journey of building a new kind of organisation. This means we’re opening new ways to work, ground-breaking methods and bringing unexpected teams together Interested? Come and join our journey! Panthera Biopartners is an equal opportunity employer. Panthera will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. Panthera only employs individuals with the right to work in the country where the role is advertised.

Job Title: Clinical Research Nurse Location: York, UK Start Date: ASAP Rate: £175-£225/day Company Overview We are proud to be partnering with a respected and innovative clinical research organisation that is committed to improving patient outcomes through high‑quality clinical trials. Our client delivers a diverse portfolio of studies within a supportive, patient‑centred environment, working to the highest ethical and regulatory standards. This is an exciting opportunity to join a forward‑thinking team that is shaping the future of clinical research. Role Overview Our client is seeking an enthusiastic and dedicated Clinical Research Nurse to support the delivery of clinical trials from study start‑up through to close‑out. This role is ideal for a confident nurse with excellent communication skills who enjoys building rapport with patients and working collaboratively within a multidisciplinary team. You will be instrumental in ensuring protocol compliance, accurate data collection and a positive patient experience throughout the study lifecycle. Key Responsibilities • Oversee clinical trial nursing activities from initiation to close‑out in accordance with ICH/GCP guidelines., • Attend Site Initiation Visits (SIVs) and remain updated on any protocol amendments., • Conduct PIV patient interest visits, providing clear and knowledgeable study information., • Support strong patient engagement and retention throughout each trial., • Collect, verify and accurately record study data in source notes and CRF/eCRF systems., • Foster a safe, professional and welcoming environment for both staff and study participants. Skills & Experience • NMC Registered Nurse with unrestricted practice., • Minimum of 2 years post‑registration experience., • Previous clinical research experience (desirable but not essential)., • Ability to work effectively within a multidisciplinary team with minimal supervision., • Strong patient‑focused approach and excellent communication skills., • Highly organised, self‑motivated and compliant with GDPR and regulatory standards. Interested? Apply now for immediate consideration or contact James Allen on +44 203 868 8607 – We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Planet Pharma is an Employment Business providing Global Staffing services.

Pfizer UK Undergraduate Programme 2026-2027Undergraduate Regulatory StrategistGlobal Regulatory SciencesRegulatory StrategyWho can apply?Applicants must be completing a placement as part of a degree course at a UK University, either through Year in Industry/Industrial Placement or Gap Year.

Job Title: Technical Coordinator Location: York Salary: £40,000 - £45,000 + Package Calibre Search are currently working alongside one of the UK's largest and most established housebuilders - a FTSE 100 listed residential developer with a nationwide presence and a strong reputation for delivering quality homes at scale. This is a fantastic opportunity to join a business that genuinely invests in its people, offering real career progression and a supportive technical environment. You'll be joining a well-resourced Technical Team working across live residential developments from inception through to completion. The package on offer includes a company car or car allowance, healthcare, life cover, contributory pension, performance bonus, and access to an employee benefits platform with high-street discounts and wellbeing support. In this role you'll take ownership of coordinating all technical information across a number of projects simultaneously - covering building design, specification, regulatory compliance and sustainability. You'll report into the Technical Director and work closely with external consultants, internal departments, and statutory bodies including NHBC/LABC and local authorities. Day to day you can expect to be managing the flow of technical information to keep projects on programme and within budget, monitoring the discharge of planning conditions, issuing construction drawings, and ensuring plot completions are progressed efficiently. Health and Safety compliance and supporting the Sales team with plot releases will also form part of the remit. To be considered, the ideal candidate will have: Previous experience within a residential developer is preferred, though strong transferable experience will be considered Solid working knowledge of Microsoft Office Strong communication skills with the ability to liaise across multiple teams and external stakeholders Full UK driving licence Calibre Search promote equality in the workplace and we welcome applications from all suitably skilled or qualified candidates regardless of their sex, race, disability, religion/beliefs, sexual orientation or age. We act as both an employment agency and employment business. TPBN1_UKTJ

Our client is looking for an immediately available Accounts Assistant to join a small and busy team based in York on a contract basis. You will support with maintaining accurate financial records, processing transactions and assisting with reporting. THE BENEFITS: Parking Pension THE ROLE: You will be supporting the Finance Manager with day-to-day accounts and administration. Duties will include: Purchase and Sales ledger Bank Recs Supporting with Payroll administration Data Entry Generic administrative support Assist with Year End activities Ensure finance transactions comply with company policies and regulatory requirements. THE COMPANY: A highly successful York based company. THE CONSULTANCY: Edwards & Pearce acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. Edwards & Pearce is an Equal Opportunities Employer. TPBN1_UKTJ

MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global development and lifecycle activities within a leading pharmaceutical organisation. EU regulatory submission experience (clinical and/or lifecycle). We have extensive functional expertise in

An experienced regulatory technologist with a minimum of 4 years in cosmetic regulatory affairs. Managing an effective global regulatory horizon scanning process to ensure our regulatory processes remain future-fit. The regulatory team is focused on both regulatory compliance and customer needs to e

As Regulatory Systems manager you will shape regulatory systems strategy, drive compliance excellence, and support business-critical decision-making across international operations. As Regulatory Systems Manager you will lead a small specialist team while overseeing regulatory systems, compliance to

Work with Regulatory Operations, Regulatory Affairs, Tech Ops, etc. Utilize regulatory/product knowledge to provide operational support to ensure that labeling materials meet regulatory and company requirements and timelines. Senior Regulatory Labelling Consultant (Labelling Strategy).

Working closely with consumer associations, regulators, policymakers and global partners in the digital finance ecosystem, and with a focus in low- and middle-income countries, the Advocacy and Regulatory EngagementLead will ensure that the voice of consumers informs digital finance reform. Proven e

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We are seeking a strategic, politically astute leader to head our Commercial & Regulatory Services, providing visible leadership, direction and operational management across the Registration, Coroner, Archives & Records Services, and Hampshire Outdoor Centres.

The Role We are seeking a Senior Regulatory Affairs & Quality Assurance Specialist with experience in the medica device industry, to support an established Quality and Regulatory team in maintaining compliance with relevant medical device and IVD standards and regulations. Job Title: Senior Regul

Our client - a modern and progressive multi office law firm and part of a Fortune 500 global listed company - are seeking an accomplished, senior lawyer—either already operating at Partner level or an enthusiastic senior lawyer ready for promotion—to join and help lead a highly regarded Crime a

Collaborate with software developers, partners and customers in analyzing requirements and preparing specificationsLeading the review and implementation of new products, including reporting requirements and key metric impact, for example, liquidity ratiosServe as the primary point of contact for fun

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MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global development and lifecycle activities within a leading pharmaceutical organisation. Regulatory Affairs Manager (EU) | Leading Pharma. Lead and support planning, coordination, and preparation

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This is an additional headcount for a well known regulatory consulting company who have been operating for the lasty 20 years supporting pharma, biotech and medical device clients across Europe and USA with challenging regulatory issues. Ensure that the content of CMC work-packages and documentation

Proven experience in regulatory affairs or regulatory intelligence within biotech, pharma or CRO environments. The Regulatory Intelligence Manager will be responsible for monitoring, analysing and communicating global regulatory developments that impact access to unlicensed medicines. Lead structure

Maintain links with external regulatory network, proactively identify training/development needs and identify opportunities to further regulatory knowledge in clinical areas. Work with the technical development and device regulatory team as required in the development of drug-device combination prod

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Research and apply regulatory intelligence and knowledge of strategic options to enable innovative regulatory pathways and solutions for complex global requirements and regulatory challenges. Provide critical support in developing global regulatory strategy, planning, and execution of global investi

Contribute to regulatory writing training and support line management responsibilities as needed. Strong technical and scientific capabilities with a proven track record in delivering high‑quality regulatory documents. Our client is a leading Medical Communications Agency is looking to hire and ex

Junior Clerk (Crime & Regulatory). As a member of our clients clerking team, you will help to provide a smooth and comprehensive clerking service to our Crime and Regulatory practising members, including careful diary management, recording of briefs and instructions, checking court listings and deal

Location: UK (multi-site flexibility)Industry: Medical DevicesEmployment Type: Full-time, PermanentA leading UK-based medical device manufacturer is seeking an experienced Risk Management Specialist to join its Quality & Regulatory team.

The team advises on the full spectrum of business crime and regulatory matters, including:. You will also play a central role in shaping the future direction, growth, and market profile of the crime and regulatory practice. Support the leadership and management of the Crime & Regulatory team.

Identify, assess, and manage regulatory compliance risks arising from suppliers, documentation gaps, or regulatory change. Experience and skills required Experience working in a regulatory, compliance, or RAQA role within the medical device sector, with direct exposure to distributor, importer, or s

Murray McIntosh is delighted to be working with CropLife UK, who are seeking a Policy and Regulation Manager to join their close-knit team.CropLife UK is the leading trade association representing the UK crop solutions sector, dedicated to promoting the crucial

Under the guidance of an experienced case manager you will provide a full range of legal support on our cases, predominantly on behalf of regulators in the healthcare sector.These regulators ensure that the public is protected and standards are maintained by investigating concerns raised regarding t

Monitor payment regulatory developments in the UK and globally and apply them to regulatory affairs. Experience in payments or financial regulatory work. Payments Legal Regulatory Lawyer – 6-12 month contract – UK based working Remote.

The Regulatory Social Care and Governance Team provide a valuable service to our Local Authority Clients across a range of different Social Care work, examples being Child Care, Adult Social Care and Education (SEN Tribunal).

My client, a well‑known Financial Services business, is looking to hire a Senior Regulatory Accountant to join their Finance team. This role supports the Financial Controller across Regulatory Reporting, Financial Controls and Performance Reporting. Preparing submissions to regulators, including F