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SERM Medical Director
GSKMedical Director leading oncology pharmacovigilance and risk management at GSK, a global biopharma company. Guiding safety signals, regulatory input, and benefit–risk decisions for clinical assets.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in pharmacovigilance, risk management, and safety evaluation for oncology assets, with a strong ability to analyze clinical data and communicate evidence-based recommendations effectively. Proven leadership in cross-functional teams and regulatory submissions enhances organizational capability and operational effectiveness.
Highest-signal resume keywords
Medical DegreePharmacovigilanceSignal DetectionClinical DevelopmentRegulatory Submissions
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Risk ManagementClinical Data AnalysisSafety EvaluationBenefit-Risk AssessmentMedical Affairs
Soft Skills
Excellent CommunicationCoaching and MentoringRelationship Building
Certifications & Qualifications
GMC Registration
Industry Keywords
OncologyClinical TrialsPost-Marketing SafetyCross-Functional TeamsSafety Review Teams
About the role
Key responsibilities & impact- Provide medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development
- Lead pharmacovigilance and risk management activities for assigned oncology assets and clinical trials
- Define and drive strategies for evaluating and managing safety issues across the clinical development lifecycle
- Analyse and interpret clinical data, literature, and emerging evidence to identify and assess safety signals
- Provide expert medical input into safety components of global regulatory submissions
- Apply clinical judgement to complex data sets and inform benefit–risk decisions
- Ensure timely escalation of safety concerns through governance processes
- Represent Safety on cross-functional Clinical Matrix and Project Teams
- Lead teams addressing urgent and complex product safety issues
- Contribute to or lead Safety Review Teams
- Build relationships across functions and geographies
- Coach and mentor colleagues and contribute to organisational capability development
- Present safety issues and recommendations to senior governance committees
- Influence development decisions through clear, evidence-based communication
- Represent GSK with regulatory authorities, external experts, and partners
- Contribute to safety strategy for clinical programmes and broader SERM activities
- Identify process improvements, innovation opportunities, and operational effectiveness enhancements
Requirements
What you’ll need- Medical degree with current GMC registration or eligibility to practise in the UK
- Relevant clinical experience
- Completion of formal postgraduate clinical training, such as residency or specialty training
- Significant experience in pharmacovigilance, drug safety, or medical affairs
- Expertise in signal detection, evaluation, and risk management
- Strong understanding of clinical development and post-marketing safety processes
- Experience working effectively in matrixed, cross-functional environments
- Excellent written and verbal communication skills
- Experience preparing medical and regulatory documents
- Strong clinical judgement and ability to deliver clear, evidence-based recommendations
Benefits
Comp & perks- Annual bonus may be offered
- Eligibility to participate in a share-based long-term incentive program
- Remote working supported
- Agile working culture and flexibility opportunities
- Support for reasonable adjustments during application or interview
- Opportunities to contribute to scientific excellence and continuous improvement
- Coaching and mentoring opportunities
- Collaborative global matrix environment