Director – Global Medical Affairs Strategy (Solid Tumors)
Company: Genmab
Job ID: R14956
Category: Medical Affairs
Location: Princeton, New Jersey, United States of America
Work Model: Hybrid / Onsite (as per business needs)
Job Overview
Genmab, a global biotechnology leader in antibody-based innovation, is seeking a Director, Global Medical Affairs Strategy – Solid Tumors to lead the development and execution of global medical strategy for oncology assets across their lifecycle.
Reporting to the Global Medical Affairs Strategy Lead (MASL), this leadership role will be responsible for aligning scientific, clinical, and commercial objectives to deliver impactful medical strategies for both primary and future indications. The role requires deep expertise in solid tumors, strong cross-functional leadership, and the ability to translate complex clinical data into actionable global medical plans.
Key Responsibilities
Lead global medical strategy and annual medical planning for assigned solid tumor assets
Develop and execute strategic and tactical Medical Affairs plans across the asset lifecycle, including indication expansion
Collaborate closely with global and regional Medical Affairs teams to ensure consistent strategy execution
Define and lead engagement strategies with global thought leaders, professional societies, institutions, and patient advocacy groups
Oversee Early Access Programs and Investigator-Initiated Trial strategies in alignment with compliance, quality, timelines, and budget requirements
Drive lifecycle management initiatives, including evidence generation and data dissemination
Partner cross-functionally with Commercial, HEOR, Field Medical, Medical Information, and Communications teams
Collaborate with Clinical Development and Medical Operations teams to support clinical trial planning and execution
Contribute to global publication strategy to ensure high-quality scientific communication
Support development of internal guidance documents, SOPs, and process frameworks
Participate in regulatory document development and review for submissions
Serve as a medical expert and reviewer on promotional and medical review committees
Inform value demonstration strategies for payers and clinical decision-makers
Lead global congress strategy planning and competitive intelligence reporting
Support and lead global cross-functional launch activities
Required Qualifications & Experience
Scientific or Medical degree required (PharmD, PhD, or MD)
Minimum 7 years of experience in Medical Affairs and/or Clinical Development within Oncology
Strong expertise in the solid tumor clinical landscape; experience in gynecological cancers is preferred
Proven experience within the biotechnology or pharmaceutical industry
In-depth understanding of Medical Affairs functions and oncology drug development
Strong strategic leadership skills with demonstrated ability to build alignment across global teams
Ability to interpret and clearly communicate clinical, HEOR, and real-world evidence data
Comprehensive knowledge of global compliance and regulatory requirements across Medical Affairs, R&D, and Commercial activities
Familiarity with evidence-based medicine, applied biostatistics, and health economics is an advantage
Excellent organizational and project management skills with the ability to manage multiple priorities
Strong written, verbal, and presentation skills
Willingness to travel domestically and internationally, including occasional weekends
Compensation (United States)
Salary Range: USD 203,840 – 305,760 annually
Final compensation will be determined based on qualifications, experience, skill set, and location. Additional incentives may include performance bonuses and long-term compensation plans.
Employee Benefits (US-Based Roles)
401(k) plan with company match
Comprehensive medical, dental, and vision insurance options
Paid vacation, sick leave, holidays, and paid parental leave
Wellness and lifestyle spending benefits
Tuition reimbursement and commuter benefits
Family care, financial wellness, and emotional well-being support programs
About Genmab
Founded in 1999 and headquartered in Copenhagen, Denmark, Genmab is a global biotechnology company dedicated to improving patient outcomes through innovative and differentiated antibody therapeutics. Its proprietary pipeline includes bispecific antibodies, antibody-drug conjugates, immune checkpoint modulators, and next-generation antibody technologies. Genmab operates across North America, Europe, and Asia-Pacific with a long-term vision to transform cancer care worldwide.
Why Join Genmab
Lead global medical strategy in high-impact oncology programs
Work at the intersection of science, strategy, and innovation
Collaborate with world-class experts across regions and functions
Contribute directly to shaping future standards of cancer care
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