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Job Description & How to Apply Below
Hybrid | Crewe | Permanent
Are you an experienced Pharmaceutical Physician ready to take on a high-impact medical leadership role?
You’ll provide expert input across pharmacovigilance, regulatory affairs, product development and commercial activities. This opportunity will also allow the individual to become a medical signatory if they’re not already, great for personal development.
You’ll be responsible for:- Medical review of ICSRs, aggregate safety reports (PSURs/PBRERs/DSURs), RMPs and benefit-risk assessments
- Supporting the QPPV and ensuring GVP compliance
- Providing medical input into regulatory submissions, clinical development documents and expert statements
- Advising on medical information, promotional materials (ABPI) and cross-functional decisions up to senior level
- Industry experience as an Pharmaceutical Physician with specific experience in a pharmacovigilance setting
- Strong knowledge of GVP, causality assessment, signal evaluation and the clinical development process
- Excellent medical writing, analytical skills and the confidence to influence at all levels
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