FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Senior Medical Director, Oncology Clinical Development – Lung
GSKSenior physician leading lung oncology clinical development at GSK, a global biopharma company. Guiding trials, safety oversight, regulatory engagement, and programme-level medical strategy.
Posted 8/13/2026full-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 expertise in oncology clinical development, including medical oversight, safety evaluation, and 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
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Data InterpretationSafety EvaluationSignal DetectionBenefit–Risk EvaluationGCPICH GuidelinesOncology Disease BiologyClinical Development ProcessesPhase I–III StudiesTechnical Diligence
Soft Skills
Stakeholder EngagementMentorshipCross-Functional CollaborationLeadershipScientific Communication
Certifications & Qualifications
Advanced Specialty TrainingFellowship
Industry Keywords
Clinical Matrix TeamHealth Authority DiscussionsAdvisory BoardsScientific CommunitiesCongress Presentations
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Provide medical oversight and clinical insight across study design, conduct, and data interpretation
- Guide medical monitoring and safety oversight across studies
- Interpret complex clinical and safety data to inform programme-level decisions
- Partner with the Senior Scientist and cross-functional teams across study execution and programme delivery
- Provide senior medical input into protocols and study design
- Serve as a senior member of the Clinical Matrix Team and influence study- and programme-level decisions
- Engage with investigators, Key External Experts, scientific leaders, advisory boards, steering committees, and scientific forums
- Provide guidance and mentorship to Medical Directors
- Guide safety-data interpretation, signal detection, escalation, and benefit–risk evaluation
- Participate in safety review forums such as SRT and IDMC
- Support complex medical questions arising during study conduct
- Contribute to data interpretation, scientific communications, publications, congress materials, and clinical summaries
- Contribute medical expertise to regulatory interactions and Health Authority discussions
- Lead or contribute to clinical and technical diligence for business development opportunities
- Contribute to disease-area strategy, integrated evidence planning, Medical Affairs discussions, and Oncology Clinical Development initiatives
- Support clinical capability development, 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 oncology, haematology, or a related specialty
- Clinical and pharmaceutical experience in oncology clinical development 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
- 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 regulatory interactions such as IND, scientific advice, and NDA/MAA
- 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 evolving treatment landscapes across solid tumours and/or haematological malignancies
- Experience mentoring or providing oversight to other physicians within a clinical development organisation
- Experience contributing to clinical and technical diligence for business development opportunities
Benefits
Comp & perks- Annual bonus
- Eligibility to participate in the 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