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About the role
Key responsibilities & impact- 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.
- Develops strategic approaches for safety issue evaluation within clinical development programmes.
- Contributes to safety components of global regulatory submissions (e.g., INDs, DSURs, IBs).
- Ensures high-quality, timely delivery while managing multiple priorities.
- Represents Safety Evaluation & Risk Management (SERM) on Clinical Matrix and Project Teams.
- Leads cross-functional efforts to address urgent and complex product safety issues.
- Partners closely with Safety Physicians and stakeholders to prepare for and contribute to Safety Review Team (SRT) meetings.
- Escalates emerging safety issues to senior leadership and governance bodies as appropriate.
- Communicates complex scientific information clearly to a range of audiences.
Requirements
What you’ll need- Degree in a health-related discipline (e.g., Life Sciences, Pharmacy, Medicine, Nursing), with significant relevant experience
- Substantial experience in pharmacovigilance, drug safety, or a related function within the pharmaceutical or biotechnology industry
- Experience supporting safety in oncology clinical development programmes
- Strong expertise in: Signal detection and risk assessment
- Clinical trial safety oversight
- Regulatory safety documentation and submissions
- Knowledge of global pharmacovigilance regulations (e.g., ICH, GVP, CIOMS)
- Proven ability to work effectively in a complex, global matrix environment
- Strong analytical, communication, and problem-solving skills.
Benefits
Comp & perks- Bonuses
- Eligibility to participate in share based long term incentive program
ATS Keywords
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Hard Skills & Tools
pharmacovigilancedrug safetysignal detectionrisk assessmentclinical trial safety oversightregulatory safety documentationglobal pharmacovigilance regulationsINDsDSURsIBs
Soft Skills
analytical skillscommunication skillsproblem-solving skillsability to work in a complex environmentleadershipcollaborationtime managementprioritization