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Medical Director, SERM
GSKSERM Medical Director at GSK providing leadership in safety evaluation and risk management of oncology assets. Leading cross-functional collaboration and ensuring patient safety in clinical development.
About the role
Key responsibilities & impact- Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development
- Responsible for the interpretation of safety data, identification and escalation of safety signals, and delivery of clear, evidence-based recommendations
- Contributes to global governance and plays a critical part in protecting patient safety and shaping the safety profile of innovative oncology medicines
- Leads pharmacovigilance and risk management activities for assigned oncology assets and clinical trials
- Defines and drives strategy for the evaluation and management of safety issues across the clinical development lifecycle
- Analyzes and interprets clinical data, literature, and emerging evidence to identify and assess safety signals
- Provides expert medical input into the safety components of global regulatory submissions
- Applies sound clinical judgement to complex and sometimes conflicting data sets to inform benefit-risk decisions
- Ensures timely escalation of safety concerns in line with governance processes
- Represents Safety on cross-functional Clinical Matrix and Project Teams
- Leads cross-functional teams to address urgent and complex product safety issues.
Requirements
What you’ll need- Medical degree with current GMC registration (or eligibility to practise in the UK)
- Completion of formal postgraduate clinical training (e.g., residency or specialty training)
- Significant experience in pharmacovigilance, drug safety, or medical affairs
- Demonstrated 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, including preparation of medical and regulatory documents
- Strong clinical judgement and the ability to deliver clear, evidence-based recommendations.
Benefits
Comp & perks- Potential for annual bonus
- Eligibility to participate in share-based long-term incentive program
- Flexible working arrangements
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
pharmacovigilancerisk managementsignal detectionclinical data analysissafety evaluationbenefit-risk assessmentregulatory submissionsclinical judgementmedical affairsclinical development
Soft Skills
leadershipcommunicationteam collaborationproblem-solvingdecision-makinginterpersonal skillsstrategic thinkingevidence-based recommendationscross-functional teamworkadaptability
Certifications
medical degreeGMC registrationpostgraduate clinical training