Associate Director – Evidence Generation
Company: Genmab
Job ID: R14941
Category: Medical Affairs
Work Model: Hybrid (Onsite minimum 60%)
Locations:
Copenhagen, Denmark
Utrecht, Netherlands
Princeton, New Jersey, USA
Job Overview
Genmab is a global biotechnology company dedicated to developing innovative antibody-based therapies that transform the treatment of cancer and other serious diseases. The company is seeking an Associate Director, Evidence Generation to play a critical role within Medical Affairs, supporting both approved and pipeline products through high-quality evidence generation initiatives.
This position will have strategic and operational responsibility for Investigator-Driven Programs, including Investigator-Sponsored Trials (ISTs), Collaborative Research Trials (CRTs), and Managed Access Programs, while ensuring compliance, scientific rigor, and cross-functional collaboration.
Key Responsibilities
Lead and oversee Investigator-Driven Evidence Generation programs across multiple molecules
Develop, implement, and manage ISTs, CRTs, and Managed Access Programs from proposal submission to study closure
Execute formal scientific and operational review processes for study proposals, protocols, and amendments
Facilitate internal and cross-functional review committee meetings and document decisions
Manage project timelines, budgets, deliverables, and performance metrics
Partner with cross-functional stakeholders including Development, Research, Legal, Finance, Supply Chain, Regulatory, and Alliance Partners
Independently manage operational aspects of ISTs, including site coordination, documentation, drug supply, and payments
Generate and present regular program metrics, reports, and insights to leadership and strategy teams
Support field-based Medical Affairs and MASL teams to achieve program objectives
Contribute to contract reviews and negotiations related to investigator-driven research
Author, review, and support SOP development, implementation, and training activities
Identify risks and proactively implement solutions aligned with global regulations and guidelines
Drive process improvements to enhance operational efficiency and compliance
Required Qualifications & Experience
Bachelor’s, Master’s, or advanced degree in a scientific discipline
Minimum 8 years of experience in the pharmaceutical or biotechnology industry
Strong preference for experience within Oncology Medical Affairs
Proven experience in program or project management involving clinical or medical research initiatives
Hands-on experience managing global Investigator-Sponsored Trials or Medical Affairs programs
Solid understanding of oncology therapeutic areas such as lymphoma, breast cancer, or solid tumors (preferred)
Experience with budgeting, financial oversight, and contract management
Strong analytical skills with experience producing and interpreting metrics and reports
Excellent organizational skills with high attention to detail and ability to manage multiple priorities
Ability to synthesize complex medical and scientific data and communicate insights clearly in written and verbal formats
Compensation (United States Only)
Salary Range: USD 171,360 – 257,040 annually
Final compensation will be based on experience, qualifications, skills, and location. Eligible roles may include additional incentives such as bonuses and long-term compensation plans.
Employee Benefits (US-Based Roles)
401(k) plan with company match
Comprehensive medical, dental, and vision insurance
Paid vacation, sick leave, holidays, and parental leave
Wellness and lifestyle spending benefits
Tuition reimbursement and commuter benefits
Family care and emotional well-being support programs
About Genmab
Founded in 1999 and headquartered in Copenhagen, Denmark, Genmab is an international biotechnology company with a strong focus on antibody innovation. With a proprietary pipeline spanning bispecific antibodies, antibody-drug conjugates, and next-generation immune modulators, Genmab’s mission is to improve patient lives through breakthrough science. The company operates globally across North America, Europe, and Asia-Pacific.
Why Join Genmab
Work in a science-driven, innovation-focused environment
Collaborate with global experts in oncology and antibody research
Contribute directly to evidence that shapes patient care worldwide
Be part of a purpose-driven organization with long-term growth ambitions
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