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GSK

Senior Global Medical Director, CKM

GSK

. Lead global Medical Affairs strategy for assigned indication-expansion opportunities .

Posted 10/27/2026full-timeLondon • United KingdomSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in leading Medical Affairs strategy for cardio-renal-metabolic indications, with a strong focus on evidence generation, scientific communication, and cross-functional collaboration. Proficient in managing complex projects and influencing stakeholders in a global matrix environment while ensuring compliance with regulatory standards.

Highest-signal resume keywords
MD/MBBS, PharmD Or PhDExperience In Cardio-Renal-Metabolic DiseaseGlobal Medical Affairs ExperienceHigh-Impact Scientific CommunicationExperience In Patient Segmentation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical DevelopmentIntegrated Evidence PlanningLifecycle StrategyRegulatory Briefing DocumentsHealth-Outcomes ResearchReal-World EvidenceEndpoint StrategyProject ManagementBudget ManagementEvidence Generation
Soft Skills
Outstanding Written CommunicationOutstanding Verbal CommunicationInfluencing Senior StakeholdersDecision-Making Under AmbiguityCollaboration
Industry Keywords
Medical GovernanceGSK Code Of PracticeSOPsHealthcare SystemsDiverse Codes Of PracticeSafety RequirementsRegulatory RequirementsMarket AccessScientific EducationPatient Pathways

About the role

Key responsibilities & impact
  • Lead global Medical Affairs strategy for assigned indication-expansion opportunities
  • Provide senior medical input to indication sequencing, target-population definition, patient segmentation, desired medicine profile, differentiation and scientific value proposition
  • Partner with Clinical Development on study design, endpoints, data interpretation and medical relevance of development choices
  • Lead or co-lead integrated evidence planning and prioritise evidence gaps across clinical outcomes, PROs, RWE, health outcomes, epidemiology, diagnostics, care pathways and implementation science
  • Drive global scientific communications including publications, congresses, advisory boards and scientific education
  • Provide Medical Affairs leadership to early cardio-renal-metabolic assets from candidate selection through Commit to Phase 3 or transition to asset-specific medical leads
  • Profile patient pathways and treatment landscapes, define unmet needs, and identify evidence and education requirements
  • Build global matrix partnerships across R&D, Evidence Generation, Global Product Strategy, Market Access, Regulatory, Safety, Finance, Procurement and country Medical teams
  • Manage project-critical resources, vendors and budgets to deliver milestones
  • Ensure appropriate medical governance and compliance with the GSK Code of Practice, SOPs and relevant external codes and regulations

Requirements

What you’ll need
  • MD/MBBS, PharmD or PhD in a clinical or scientific discipline
  • Experience in cardio-renal-metabolic disease, with direct clinical or scientific work in this area
  • Experience in Medical Affairs at global and/or major-market level, with strategic responsibility for an asset or disease area
  • Experience supporting all stages of clinical development, integrated evidence planning and lifecycle strategy
  • Experience translating external medical insights and complex evidence into asset strategy, development decisions and executable medical plans
  • Experience leading within a global matrix, influencing senior cross-functional stakeholders and driving decisions under ambiguity without direct line authority
  • Experience managing multiple concurrent projects, budgets, vendors and priorities in a fast-paced global environment
  • Experience in high-impact scientific communication, with outstanding written and verbal communication skills in English
  • Experience with pre-launch and launch preparation at both global and local level
  • Experience in patient segmentation, endpoint strategy, real-world evidence, health-outcomes research or implementation science
  • Experience contributing to regulatory briefing documents, payer dossiers, guideline-shaping evidence or post-approval commitments
  • Experience evaluating early assets or business-development opportunities in cardio-renal-metabolic disease
  • Robust understanding of diverse healthcare systems, internal and external codes of practice, safety and regulatory requirements, and applicable industry standards

Benefits

Comp & perks
  • Agile working culture and flexibility opportunities
  • Equal opportunity employment
  • Adjustments/support available during the recruitment process