GSK
SERM Scientific Director, Oncology
$170K–$283K
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
- Advanced experience: 5+ years in the Pharmaceutical or Biotech industry working in Pharmacovigilance or Drug Safety.
- Education
- Bachelor of Science in Life Sciences or Medical Sciences (minimum standard); PharmD/PhD for Scientist (preferred).
About the job
Leads oncology pharmacovigilance and risk management, overseeing safety evaluation, governance, regulatory submissions, and risk-reduction strategies across clinical development and post-marketing products.
What you'll do
- Develops pharmacovigilance and risk management strategy, evaluates safety data, and leads safety components of global regulatory submissions.
- Leads cross-functional safety governance, detects and addresses product safety issues, and ensures risk-reduction strategies are implemented.
- Presents safety recommendations to senior governance groups and represents GSK in regulatory and external discussions.
What they ask for
- Bachelor of Science in Life Sciences or Medical Sciences (minimum standard); PhD/PharmD preferred for Scientist.
- Advanced experience (5+ years) in the Pharmaceutical or Biotech industry in Pharmacovigilance or Drug Safety.
- Significant pharmacovigilance experience in Safety Evaluation and Risk Management, covering clinical development and post-marketing activities.
- Experience with Signal Detection and safety surveillance; knowledge or experience of international pharmacovigilance requirements and drug development and approval processes.
Nice to have
- PharmD/PhD for Scientist.
- Experience working in large matrix organizations.
Pay
$169,950 to $283,250 USD annual base salary
Model-written summary · the original posting is authoritative