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GSK

Global Medical Director, Oncology

GSK

. Lead development and delivery of the global medical affairs plan and integrated evidence plan for oncology assets .

Posted 9/18/2026full-timeUpper Providence • North Carolina • United StatesLeadWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading global medical affairs strategies and evidence generation in oncology, with a strong focus on clinical trial design and stakeholder engagement. Proficient in providing medical governance and ensuring compliance in scientific communications.

Highest-signal resume keywords
MD, PharmD, Or PhD5+ Years' Experience In Medical AffairsGlobal Medical StrategiesClinical Trial DesignExcellent Written And Verbal Communication

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Medical AffairsClinical DevelopmentEvidence GenerationOncologyClinical Trial DesignScientific EngagementData Presentation
Soft Skills
CommunicationCollaborationAdaptability
Industry Keywords
Oncology AssetsAdvisory BoardsCongress StrategyScientific EducationRegulatory Engagement

About the role

Key responsibilities & impact
  • Lead development and delivery of the global medical affairs plan and integrated evidence plan for oncology assets
  • Drive above-country medical activities, including advisory boards, congress strategy, symposia, and scientific education
  • Own scientific engagement with external experts, patients, payers, and regulators
  • Partner with research and development to design and prioritize global and supportive clinical studies
  • Review investigator-initiated proposals
  • Support brand and launch planning by providing medical input to local operating companies and commercial teams
  • Provide medical governance and review scientific materials for accuracy, compliance, and clear communication
  • Shape evidence generation and translate clinical insights into patient impact

Requirements

What you’ll need
  • MD, PharmD, or PhD with relevant clinical or scientific experience in oncology
  • 5+ years' experience in medical affairs, clinical development, or related roles in Oncology
  • Demonstrated experience leading global medical strategies and evidence generation plans
  • Strong understanding of clinical trial design and operational experience with global studies
  • Experience engaging external experts, advisory boards, and congress planning
  • Excellent written and verbal communication in English and proven ability to present complex data clearly
  • Ability to work in a hybrid environment with remote and on-site work
  • Willingness to travel to meet colleagues, partners, and external experts

Benefits

Comp & perks
  • Comprehensive benefits program for US employees
  • Recruitment-process accommodations and assistance for inclusion
  • Equal opportunity employment