Medical Information & Pharmacovigilance Specialist / London / 40k to 50k per annum (pro rata) DOE
Part-time, temporary 6-month contract, 3 days per week (22.5 hours), hybrid working arrangement.
About the Role
Our client, a leading pharmaceutical organisation specialising in Dermatology, is currently recruiting an experienced candidate to support pharmacovigilance and medical information functions. The role involves managing inquiries, adverse event reports, and ensuring compliance with regulatory standards.
Key Responsibilities
1. Manage mailbox and triage reports for adverse events (AEs), medical inquiries (MIs), and product quality complaints (PQCs).
2. Respond to medical information requests following SOPs and regulatory guidelines.
3. Log and follow up on adverse event reports.
4. Ensure compliance with Good Pharmacovigilance Practices (GVP).
5. Support product quality complaint logging and corporate PV follow-ups.
Requirements
1. Degree in medicine, pharmacy, or biosciences.
2. 1-2 years of industry experience, especially in adverse event case management.
3. Strong communication skills, attention to detail, and a proactive attitude.
Note: The phrase "PRESENT" appears to be an error or placeholder and has been omitted.
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