Pharmaceutical Physician & Medical Advisor (Hybrid)

Cpl Life Sciences; Crewe; Hybrid; GBP 60,000 - 90,000; Full time

Job summary

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.

Qualifications

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

Responsibilities

• 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

Skills

Pharmacovigilance

Medical writing

Regulatory submissions

GVP knowledge

Influence at senior levels

Job description

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.