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ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
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
Industry Keywords
oncologysafety evaluationrisk managementclinical developmentsafety review teamglobal regulatory submissionssafety issuesstakeholder engagementmatrix environmentpatient safety
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