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.
• Partners cross-functionally to ensure high-quality, timely decision-making and proactive risk mitigation across the portfolio.
• Represents Safety Evaluation & Risk Management (SERM) on Clinical Matrix and Project Teams.
• Leads cross-functional efforts to address urgent and complex product safety issues.
• Prepares and presents at Safety Review Team (SRT) meetings.

• 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.