SERM Scientific Director

Responsibilities

• Provides advanced scientific expertise in the safety evaluation and risk management of key GSK oncology assets in clinical development.
• Leads the identification, assessment, and communication of safety risks to ensure robust benefit‑risk profiles and protection of patients globally.
• Drives the evaluation and interpretation of safety data, including signal detection and assessment.
• Mentors and coaches junior team members as applicable.

• Degree in a health or life sciences discipline (e.g., Bachelor of Science, PharmD, MD, PhD, or equivalent).
• Minimum 5 years experience in pharmacovigilance, drug safety, or related safety evaluation role in the pharmaceutical or biotech industry.
• Practical experience in signal detection, safety surveillance and risk management across clinical development and post‑marketing.
• Knowledge of global pharmacovigilance requirements and drug development processes.
• Strong clinical or scientific judgement with experience interpreting clinical and safety data.
• Certifications:
  
  Bachelor of Science, PharmD, MD, PhD.