Oncology Safety Strategy Director (SERM) - Hybrid US

GlaxoSmithKline; Rockville (MD); Hybrid; USD 223,000 - 371,000; Full time

Benefits offered by this job

Health insurance

Retirement benefits

Paid holidays

Job summary

GlaxoSmithKline in the United States seeks a Medical Safety Leader to provide medical and scientific leadership in safety evaluation and risk management for oncology assets in clinical development. You will interpret safety data, escalate signals, and deliver clear, evidence‑based recommendations to support benefit‑risk decisions.

This role is hybrid and based in the US. This position requires a medical degree and postgraduate clinical training, extensive pharmacovigilance experience, and the

Qualifications

• Medical degree with clinical training and GMC eligibility.
• Significant pharmacovigilance or drug safety experience.
• Strong ability to interpret complex clinical data and communicate findings.

Responsibilities

• Lead pharmacovigilance and risk management activities for oncology assets.
• Define strategy for safety evaluation across the development lifecycle.
• Provide expert input into safety components of regulatory submissions.
• Lead Safety Review Teams and cross-functional safety collaboration.

Skills

Analytical Thinking

Clinical Data Interpretation

Clinical Development

Clinical Pharmacology

Clinical Trial Designs

Clinical Trials Monitoring

Digital Fluency

Drug Regulatory Affairs

Evidence Based Decision Making

Executive Presence

Hematology and Oncology

Learning Agility

Matrix Leadership

Real World Evidence

Scientific Presentations

Education

Medical degree with GMC registration / eligibility

Postgraduate clinical training (residency or specialty)

Job description

GlaxoSmithKline in the United States seeks a Medical Safety Leader to provide medical and scientific leadership in safety evaluation and risk management for oncology assets in clinical development. You will interpret safety data, escalate signals, and deliver clear, evidence‑based recommendations to support benefit‑risk decisions.

This role is hybrid and based in the US. This position requires a medical degree and postgraduate clinical training, extensive pharmacovigilance experience, and the