Senior SERM Director, Oncology Safety & Risk Strategy

GSK plc

Oaks (PA)

Hybrid

USD 218,000 - 363,000

Full time

5 days ago
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Benefits offered by this job

Health care and other insurance
Retirement benefits
Paid holidays
Vacation
Paid caregiver/ parental and medicalle

Job summary

GSK plc is seeking a Scientific Director specializing in safety evaluation for oncology assets. The role leads pharmacovigilance activities, risk mitigation, and safety data interpretation across clinical development.

You will collaborate across functions to shape safety strategy and contribute to regulatory submissions. The position is hybrid in the United States, with on-site governance meetings and remote work balance.

Qualifications

  • Bachelor's or higher in health or life sciences.
  • 5+ years in pharmacovigilance, drug safety, or related safety evaluation role.
  • Knowledge of global pharmacovigilance requirements and drug development processes.

Responsibilities

  • Lead pharmacovigilance activities and risk mitigation for oncology assets and trials.
  • Drive evaluation and interpretation of safety data, including signal detection.
  • Develop strategic approaches for safety evaluation within development programs.
  • Contribute to safety components of global regulatory submissions (INDs, DSURs, IBs).
  • Perform literature reviews, data synthesis, and integrated safety analyses.
  • Ensure timely outputs while managing multiple priorities.
  • Represent Safety Evaluation & Risk Management on Clinical Matrix/Projects.
  • Lead cross-functional efforts to address safety issues and mentor team members.

Skills

Digital Fluency
Enterprise Leadership
Influencing Without Authority
Pharmacovigilance
Presentation Techniques

Education

Bachelor's degree in health or life sciences
Advanced degree (PharmD, PhD, MD) preferred

Job description

GSK plc is seeking a Scientific Director specializing in safety evaluation for oncology assets. The role leads pharmacovigilance activities, risk mitigation, and safety data interpretation across clinical development.

You will collaborate across functions to shape safety strategy and contribute to regulatory submissions. The position is hybrid in the United States, with on-site governance meetings and remote work balance.

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