6 month temporary contract
Our client, a leading pharmaceutical organisation specialising in dermatology, is seeking an experienced Medical Information & Pharmacovigilance Specialist to support their medical information and safety operations. This position is suited to a detail‑oriented professional with hands‑on experience in adverse event case management and a strong understanding of Good Pharmacovigilance Practices.
Role Overview
You will manage medical information enquiries, triage mailbox reports, log adverse events, and ensure full compliance with UK and international regulatory standards. This role is central to maintaining high‑quality medical information delivery and supporting patient safety activities.
Key Responsibilities
Mailbox management - triage incoming reports to identify Adverse Events (AEs), Medical Information (MIs) queries, and Product Quality Complaints (PQCs).
Medical information responses - log and respond to enquiries using approved documentation, SOPs, WIs, and regulatory guidelines.
Adverse event reporting - log, assess, and follow up AE reports in accordance with SOPs, WIs, and GVP requirements.
Regulatory compliance - ensure all activities meet Good Pharmacovigilance Practices and relevant local/international regulations.
Product quality complaint logging - support PQC documentation when required.
Corporate PV follow‑up - contribute to ongoing safety follow‑up requests from global pharmacovigilance teams.
Profile Requirements
Degree in medicine, pharmacy, or biosciences.
Experience in adverse event case management within the pharmaceutical industry.
1-2 years' experience in medical information, pharmacovigilance, or a related field.
This is a 6 month temporary contract
37.5 hours per week Monday to Friday
Hybrid, 3 days per week on site in Euston, London
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Salary description
£28.50 - £28.50 per hour