FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
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 Director, Global Medical Director – GI Tumors
Jazz Pharmaceuticals. Lead the GI Cancer Global Medical functional matrix team .
Posted 11/3/2026full-timeRemote • Pennsylvania • United States, United Kingdom, CanadaSenior💰 $268,000 - $402,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in Medical Affairs and Clinical Development, particularly in oncology and GI cancers, with a strong focus on evidence generation strategies and stakeholder engagement. Proven ability to lead cross-functional teams and manage complex projects in a fast-paced environment.
Highest-signal resume keywords
Medical Affairs LeadershipOncology Drug DevelopmentEvidence-Generation StrategyStakeholder ManagementLifecycle Management
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 ResearchEvidence GenerationPublication PlanningOncology ExperienceStrategic ThinkingOperational ExecutionAnalytic Needs IdentificationTrial DesignHealth Outcomes ResearchPhase IV Interventional Studies
Soft Skills
Influencing Without AuthorityPartnership BuildingManaging Multiple PrioritiesExcellent CommunicationPresentation Skills
Certifications & Qualifications
Advanced Scientific Degree (PharmD, PhD, MD, MBBS, Nurse Practitioner, PA)
Industry Keywords
GI CancersHER2-Targeted TherapiesIntegrated Evidence Generation PlanCross-Functional TeamsReal-World EvidenceClinical DevelopmentMarket AccessRegulatory AffairsCommercial EngagementOncology Care Delivery
About the role
Key responsibilities & impact- Lead the GI Cancer Global Medical functional matrix team
- Partner with US and EUR/INT Medical Affairs teams to understand regional customer, patient, healthcare provider, and healthcare system needs and priorities
- Represent and advocate for medical perspectives within global cross-functional teams and governance forums, including CDT, LDT, PGC, and DPRC
- Contribute Medical Affairs expertise to early development activities, including TPP development, clinical trial design, and lifecycle planning
- Ensure regional needs and insights are considered in clinical development discussions, evidence-generation activities, and lifecycle planning
- Maintain and apply understanding of the competitive landscape to inform evidence-generation strategy and internal development decisions
- Lead development, maintenance, and execution of the Integrated Evidence Generation Plan for solid tumor oncology products in BTC, gastroesophageal cancer, and other GI malignancies
- Partner across Medical Affairs, Clinical Development, Regulatory Affairs, Market Access, HEOR, RWE, Commercial, and other cross-functional teams
- Lead and support evidence-generation activities, including investigator-sponsored studies, real-world evidence initiatives, health outcomes research, and Phase IV interventional studies
- Lead development of the breast cancer medical narrative by identifying and advancing analytic needs and informing interpretation of pivotal trial data
- Provide Medical Affairs leadership and input into the Payor Value and Evidence Plan
- Lead development and execution of publication strategy and evidence dissemination plan
- Support scientific communications, congress planning, advisory boards, and external engagement activities
- Act as a subject matter expert for internal cross-functional stakeholders
Requirements
What you’ll need- Minimum of 10 years of Medical Affairs, Clinical Development, or related pharmaceutical or biotechnology industry experience
- Oncology experience preferred
- Experience in GI cancers and/or HER2-targeted therapies strongly preferred
- Experience developing and executing evidence-generation strategies, publication plans, and external scientific engagement activities
- Strong understanding of clinical research, evidence generation, and oncology drug development
- Ability to influence without authority and operate effectively within complex matrix organizations
- Strong strategic thinking and operational execution skills
- Excellent written, verbal, presentation, and stakeholder management skills
- Ability to build productive partnerships across regions and functions
- Ability to manage multiple priorities and deliver high-quality outcomes in a fast-paced environment
- Experience in lifecycle management of oncology indications strongly desired
- Advanced scientific or healthcare degree required (PharmD, PhD, MD, MBBS, Nurse Practitioner, PA, or equivalent)
- Experience in delivery of oncology care preferred
Benefits
Comp & perks- Discretionary annual cash bonus or incentive compensation
- Discretionary equity grants through the Long Term Equity Incentive Plan
- Medical insurance
- Dental insurance
- Vision insurance
- 401k retirement savings plan
- Flexible paid vacation