Pharmaceutical Physician

Cpl Life Sciences; Crewe; Híbrido; GBP 60 000 - 90 000; Tempo integral

Resumo da oferta

CPL Life Sciences in Crewe is seeking an experienced Pharmaceutical Physician to lead medical input across pharmacovigilance, regulatory affairs, product development and commercial activities in a hybrid Crewe-based role.

The successful candidate will become a medical signatory if not already, and will support QPPV, RMPs, PSURs and DSURs, contributing to benefit-risk assessments and regulatory decisions.

Qualificações

• Pharmacovigilance experience within pharmaceutical medicine.
• Strong medical writing and analytical capabilities.
• Knowledge of GVP and regulatory processes.

Responsabilidades

• 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, ABPI-compliant promotional materials and cross-functional decisions at senior levels
• Industry experience as a Pharmaceutical Physician with pharmacovigilance focus
• Strong knowledge of GVP, causality assessment, signal evaluation and the clinical development process
• Excellent medical writing, analytical skills and ability to influence at all levels

Conhecimentos

Pharmacovigilance

Medical writing

Regulatory submissions

GVP knowledge

Influence at senior levels

Descrição da oferta de emprego

Pharmaceutical Physician / Medical Advisor

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