Pharmacovigilance jobs in AndoverCreate job alerts

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 are seeking a highly motivated and detail-oriented physician to join our growing Drug Safety & Pharmacovigilance team as a Director of Medical Safety. In this role, you will play a key function in ensuring the safety of our marketed drugs and contribute to the development and implementation of ph

You will take ownership of end-to-end case processing oversight, ensuring compliance with global pharmacovigilance regulations while leading and developing a high-performing team. Strong experience in pharmacovigilance (CRO and/or MAH environment). We’re supporting a growing, international pharma

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

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

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

Cookie NoticeDirector, Pharmacovigilance (LPVM) UK/IRL & UK Qualified Person for Pharmacovigilance (UK QPPV) page is loaded## Director, Pharmacovigilance (LPVM) UK/IRL & UK Qualified Person for Pharmacovigilance (UK QPPV)locations: London (UK)time type: Full timeposted on: Posted Todaytime lef

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 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.

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

Maintain inspection-ready safety documentation, including case records and Trial Master File (TMF) components, and lead or support regulatory inspections, audits, and internal quality reviews from a pharmacovigilance perspective. Support safety data reconciliation activities between pharmacovigilanc

Ennov’s cloud-based solutions cover Regulatory Affairs, Pharmacovigilance, Quality, Clinical, and Document Management. 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 Pharm

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 is looking for a professional to provide medical expertise in pharmacovigilance.

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

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

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

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

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

A global biopharmaceutical company is seeking a Director, Pharmacovigilance to lead and oversee the PV operations across the UK & Ireland.

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.

Prior experience in medical information or pharmacovigilance is preferred.

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

Review and summarize scientific literature relevant to pharmacovigilance. Strong knowledge and understanding of international safety reporting and pharmacovigilance requirements and signal detection. We are seeking a highly motivated and detail-oriented physician to join our growing Drug Safety & Ph

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

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