Trabajos pharmacovigilance en HarpendenCrear alertas

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

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

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 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 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 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 & What You Will Be Doing* Ensuring pharmacovigilance obligations are consistently and adequately considered for all new/updated/terminated business relation

The role involves leading the design and continuous improvement of global safety processes and requires extensive experience in Pharmacovigilance, Signal Management, and Risk Management.

Reviewing contractual business agreements (“Main Agreements”) and determining whether inclusion of Pharmacovigilance language is required and, if yes, whether a standalone Pharmacovigilance Agreement (PVA) is needed. Ensuring pharmacovigilance obligations are consistently and adequately consider

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

Demonstrate ability to learn quickly, adapt to a new process, and/or develop expertise in pharmacovigilance practices and safety regulations. Prior experience in pharmacovigilance, drug safety, Safety Evaluation and Risk Management, benefit-risk evaluation, aggregate safety reports, clinical develop

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

The Senior Pharmacovigilance (PV) Operations Specialist will have prior experience in preparing the safety data package for submission to regulatory authorities (e. Maintain inspection-ready safety documentation, including case records and Trial Master File (TMF) components, and lead or support regu

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

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.

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. We have a vacancy for a Senior Veterinary Pharmacovigilance Assessor. Stay informed on

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

Prior experience in medical information or pharmacovigilance is preferred.

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

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

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

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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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