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Experienced Pharmacovigilance Lead (Hybrid role) This is NOT an entry level role. At least 3-5 years PV experience in a CRO is required. 6 month initial Fixed Term Contract Immediate start preferred The Pharmacovigilance Lead provides operational and scientific leadership for assigned projects and/or functional PV activities, ensuring delivery of high‑quality, compliant PV services in accordance with the TMC PV QMS, contractual obligations, and regulatory expectations. THIS IS A HYBRID ROLE: we expect the successful candidate be able to come to the office in Hartley Wintney, Hampshire, at least twice a week. Role-specific tasks include; Case processing, reporting and team management • Responsible for day-to-day oversight of end-to-end case processing, including management of PV rota, functional guidance, and leadership of case processing team, • Management of case-processing flow, ensuring regulatory reporting compliance., • Oversight of case-processing KPIs and maintaining and reporting on internal metrics and KPIs, • Provide expertise, support and active participation in case processing and routine departmental PV activities (e.g. MedDRA coding, eTMF, reconciliations), • Support PV Manager in preparation and maintenance of key client documentation (e.g. SMPs and PSMFS), • Ensure PV deliverables are executed, and delivered in compliance with the TMC PV QMS, SOPs, and applicable regulations., • Ensure inspection readiness for assigned projects, including support for audits and regulatory inspections., • Review and approve PV documents (inc. Project-specific and departmental controlled documents), reports, and outputs in line with delegated authority., • Support PV managers as point of contact for assigned clients or internal stakeholders., • Support PV governance activities, including oversight meetings, metrics review, and performance reporting. Other key information: Education and experience • Advanced life sciences degree (or equivalent experience)., • Significant experience in pharmacovigilance within a CRO and/or MAH environment., • Proven leadership and decision‑making capability., • Strong regulatory and scientific judgement., • Excellent stakeholder and client management skills., • Ability to balance operational delivery with quality and compliance oversight.

With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-prof

We’re supporting a growing, international pharma organisation in their search for an experienced Pharmacovigilance Team Lead to join their expanding PV function. You will take ownership of end-to-end case processing oversight, ensuring compliance with global pharmacovigilance regulations while lea

A government agency in the UK is seeking a Senior Veterinary Pharmacovigilance Assessor responsible for post-authorisation surveillance of veterinary medicines.

A global biopharma company in London is seeking a Pharmacovigilance Scientist with expertise in safety evaluation and risk management.

Our client is currently seeking a Pharmacovigilance Manager in UK. Responsible for designing, implementing, and managing pharmacovigilance strategies and activities. Collaborate with cross-functional teams, regulatory authorities, and external partners to maintain a comprehensive pharmacovigilance s

A leading global biopharma company is seeking a safety evaluation expert to lead pharmacovigilance and risk management activities.

A global biopharma company is looking for a professional to provide medical expertise in pharmacovigilance.

Develop, maintain, and provide training on SOPs, PV processes, and procedures in accordance with Good Pharmacovigilance Practices (GVP)* Collaborate with cross-functional teams (clinical operations, regulatory affairs, medical affairs) to address safety issues and develop effective risk minimization

A global pharmaceutical company is seeking a Pharmacovigilance and Risk Management expert to lead safety evaluations and regulatory submissions.

A leading pharmaceutical company seeks a Senior Pharmacovigilance Officer in Reading, UK.

A leading provider of pharmacovigilance solutions in the United Kingdom is seeking a Consulting Technology Project Manager. The ideal candidate will have over 8 years of project management experience, specifically in pharmacovigilance or regulatory technology projects.

A global pharmaceutical company is seeking a Pharmacovigilance Associate in Gloucestershire. Ideal candidates will have experience in pharmacovigilance, exceptional communication skills, and the ability to build strong relationships across teams.

A global biopharmaceutical company in Greater London is seeking an experienced professional to lead Pharmacovigilance and Risk Management.

A leading training organization in the United Kingdom is seeking a Pharmacovigilance Course Lead to design and deliver an industry-focused training program. This fully remote role requires 7–10+ years of experience in Pharmacovigilance and a strong ability to mentor future professionals.

The role We’re looking for an experienced Medical Officer providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP), Epidemiology, Medical Affairs, and Medical & Process Compliance. Key responsibilities* Lead and develop high-performing GCSP, Epidemiology, Medical

Strong knowledge of global pharmacovigilance regulations (FDA, EMA, ICH, CIOMS). The Senior Pharmacovigilance (PV) Operations Specialist will have prior experience in preparing the safety data package for submission to regulatory authorities (e. Provide oversight and governance of the CellCentric ph

Sales Executive – Pharmacovigilance/Clinical Trial IT Solutions (Life Sciences). Reporting to our VP of Sales & Marketing in Paris, you will be responsible for selling our Pharmacovigilance and Clinical Trials solutions to clients in the life sciences and healthcare sectors located in Europe, and

Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally. Demonstrate ability to learn quickly, adapt to a new process, and/or develop expertise in pharmacovigilance practices and safety regulations. Prior experienc

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A leading life science consulting firm in the United Kingdom is seeking a Pharmacovigilance Manager to design and manage pharmacovigilance strategies.

As a senior member of the Pharmacovigilance (PhV) team within the Authorisations Division, you will help protect animal, environmental and public health through a globally recognised approach to pharmacovigilance. Stay informed on developments in pharmacovigilance and veterinary medicines regulation

We are currently looking to partner with Pharmacovigilance (GVP) Auditor who can partner with us to perform a critical GVP audit for one of our key clients in Quarter 2 2026 (dates are flexible within the period). Extensive experience in Pharmacovigilance (GVP) auditing is required with the life-sci

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