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CHM's Pharmacovigilance Expert Advisory Group; PEAG

Job in City of Westminster, Central London, Greater London, England, UK
Listing for: Medicines and Healthcare products Regulatory Agency
Full Time position
Listed on 2026-01-26
Job specializations:
  • Healthcare
    Medical Science Liaison, Pharmacy Technician, Healthcare Compliance
Job Description & How to Apply Below
Position: CHM's Pharmacovigilance Expert Advisory Group (PEAG)
Location: City of Westminster

The PEAG also advises the CHM and the Medicines and Healthcare products Regulatory Agency (MHRA) on the strategic direction of the Yellow Card Scheme – the UK system for collecting and monitoring information on suspected adverse effects and medicine‑related safety concerns, and provides advice to MHRA on public applications for access to Yellow Card data for scientific research.

We are looking for an experienced community/hospital pharmacist who can provide their specialism’s perspective on relevant UK clinical practice and medicine‑related matters. The applicant must be registered with the General Pharmaceutical Council (GPhC) and currently practising as a community or hospital pharmacist, preferably with an interest in medicines safety and management and patient safety.

The Member must be able to demonstrate the qualities, skills and experience to meet all the essential criteria for appointment.

The Commission on Human Medicines (CHM) is looking to appoint one expert to the Pharmacovigilance Expert Advisory Group (PEAG).

The PEAG advises the CHM on all aspects of pharmacovigilance for human medicines (including herbal products) and vaccines. Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine‑related problem.

The PEAG advises the CHM on the public health importance of potential new safety signals; the confirmation of identified risks and their size and nature; how the risks should be managed including healthcare professional, patient and public communications; risk management planning for new and novel medicinal products; the design and progress of safety studies and analysis of the results; and methodologies for pharmacovigilance.

The Medicines and Healthcare products Regulatory Agency enhances and improves the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research.

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