Drimva

GSK

SERM Medical Director, Oncology

$223K–$371K

USA - Pennsylvania - Upper Providence +3 · Hybrid (Remote & On-site) · Director · Full-time · Posted Oct 27, 2026

Location
USA - Pennsylvania - Upper Providence
USA - Massachusetts - Waltham
Rockville Tower Oaks Blvd
Durham Blackwell Street
Experience
No specific number of years stated; significant experience in pharmacovigilance, drug safety, or medical affairs is required.
Education
Medical degree; formal postgraduate clinical training (e.g., residency or specialty training).

About the job

Leads medical and scientific safety evaluation and risk management for GSK oncology assets in clinical development, supporting patient safety and benefit–risk decisions.

What you'll do

  • Lead pharmacovigilance and risk management activities, interpret safety evidence, and identify and escalate safety signals.
  • Provide medical input to regulatory submissions and present evidence-based recommendations to governance committees.
  • Represent Safety on cross-functional teams, lead responses to complex safety issues, and coach colleagues.

What they ask for

  • Medical degree with current GMC registration or eligibility to practise in the UK, and relevant clinical experience.
  • Formal postgraduate clinical training, such as residency or specialty training.
  • Significant experience in pharmacovigilance, drug safety, or medical affairs, with expertise in signal detection, evaluation, and risk management.
  • Strong understanding of clinical development and post-marketing safety processes; effective matrix collaboration and excellent communication skills.

Nice to have

  • Postgraduate specialisation in a clinical discipline or pharmaceutical medicine.
  • Experience with regulatory submissions, safety reports, Safety Review Teams, regulatory authorities, or coaching colleagues.

Pay

$222,750 to $371,250 USD annual base salary

Model-written summary · the original posting is authoritative

First seen Oct 28, 2026 · Last verified Nov 6, 2026 (UTC)