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Senior Medical Director, Oncology Clinical Development – Sarcoma
GSKSenior Medical Director leading medical oversight for GSK’s sarcoma oncology clinical development. Guiding studies, safety, regulatory engagement, and programme strategy.
Posted 9/11/2026full-timeWaltham • Massachusetts, Pennsylvania • 🇺🇸 United StatesSenior💰 $284,250 - $473,750 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in Oncology Clinical Development, including medical oversight, safety evaluation, and clinical data interpretation. Proven ability to engage with stakeholders and contribute to regulatory interactions and scientific communications.
Highest-signal resume keywords
Medical DegreeOncology Clinical DevelopmentMedical MonitoringRegulatory InteractionsScientific Communication
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Data InterpretationSafety EvaluationDrug DevelopmentSignal DetectionBenefit–Risk EvaluationProtocol DevelopmentClinical Study DesignGCP GuidelinesICH GuidelinesClinical Diligence
Soft Skills
Stakeholder EngagementMentoringTeam CollaborationLeadership
Certifications & Qualifications
Advanced Specialty TrainingFellowship in Medical Oncology
Industry Keywords
Sarcoma OncologySoft Tissue SarcomaOsteosarcomaPhase I–III StudiesHealth Authority DiscussionsScientific PublicationsAdvisory BoardsClinical Matrix Team
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Serve as a senior physician leader within the clinical programme, providing medical oversight and clinical insight across study design, conduct, and data interpretation.
- Provide guidance on medical monitoring and safety oversight across studies.
- Interpret complex clinical and safety data to inform programme-level decisions led by the CDL.
- Partner with the Senior Scientist and cross-functional teams across study execution and programme delivery.
- Provide senior medical input into protocol development and study design.
- Serve as a senior member of the Clinical Matrix Team, influencing study-level and programme-level decisions.
- Engage with investigators, Key External Experts, and scientific leaders at advisory boards, steering committees, and scientific forums.
- Mentor Medical Directors and support development of clinical capability.
- Guide safety-data interpretation, signal detection, escalation, and benefit–risk evaluation.
- Contribute to safety review forums such as SRT and IDMC.
- Support resolution of complex medical questions during study conduct.
- Interpret clinical data across studies and contribute to scientific communications, publications, congress materials, and clinical summaries.
- Contribute to regulatory interactions and Health Authority discussions.
- Lead or contribute to clinical and technical diligence for business development opportunities.
- Contribute medical expertise to disease area strategy, integrated evidence planning, and Medical Affairs discussions.
- Lead or contribute to Oncology Clinical Development-wide initiatives and workstreams.
- Contribute to talent development, performance discussions, and capability building.
Requirements
What you’ll need- Medical degree and completion of advanced specialty training, fellowship or country-equivalent higher-level qualification in medical oncology, pediatric oncology or hematology.
- Experience in sarcoma oncology, including leading drug development.
- Clinical and pharmaceutical experience in oncology clinical development, with depth across multiple studies or programmes.
- Experience in medical monitoring, safety evaluation, and clinical data interpretation across clinical studies.
- Understanding of clinical development processes, GCP, ICH guidelines, and global regulatory frameworks.
- Experience operating within cross-functional matrix teams and contributing to complex clinical and programme-level decisions.
- Deep expertise in soft tissue sarcoma and osteosarcoma, including experience leading or supporting clinical development programs across early and/or late-stage clinical studies.
- Strong scientific communication and stakeholder engagement skills.
- Deep experience in oncology clinical development across multiple studies or programmes, including Phase I–III.
- Experience contributing to or leading aspects of regulatory interactions (e.g., IND, scientific advice, NDA/MAA).
- Demonstrated experience engaging with KEEs, advisory boards, and scientific communities in oncology.
- Track record of scientific publications and congress presentations.
- Deep understanding of oncology disease biology and the evolving treatment landscape across solid tumours and/or haematological malignancies.
- Experience contributing to clinical and technical diligence for business development opportunities.
Benefits
Comp & perks- Annual bonus
- Eligibility to participate in a share based long term incentive program
- Health care and other insurance benefits (for employee and family)
- Retirement benefits
- Paid holidays
- Vacation
- Paid caregiver/parental and medical leave
- Agile working culture and flexibility opportunities
- Equal opportunity employment