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.
Requirements
- 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.
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