Associate Director, CORE - Solid Tumors
Listed on 2026-07-14
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Research/Development
Clinical Research
Associate Director, Center for Outcomes Research (CORE) – Solid Tumors
Global role supporting Genmab's solid tumor program.
Work arrangementThis role offers flexibility to work away from the office for 20%–40% of a typical schedule. Employees may use this work schedule in increments of single days or multiple consecutive days, provided it does not exceed 40% within a 60‑day period, and is approved by the hiring manager.
Responsibilities- Implement strategies to demonstrate the unmet need in disease/value of products with a focus on outcomes meaningful to payers, clinical decision‑makers, and regulators.
- Generate the evidence necessary, through research, to maximize the commercial value of product(s) by demonstrating product differentiation and economic value.
- Support development team needs including real‑world evidence and epidemiology data to support safety.
- Manage multiple projects and product budgets to target as directed and interact with vendors in the execution of CORE projects.
- Interact with key customers (e.g., MCOs, Center for Medicare & Medicaid Services (CMS), medical experts, HTA bodies for scientific advice etc.) as needed to deliver value messages for product pricing and reimbursement, and optimal utilization.
- Actively collaborate with cross‑functional teams in development, commercial, market access, safety, legal and medical affairs to ensure alignment as required.
- Develop communication/publication strategies for given product and publish and present research outcomes at scientific conferences and forums.
- Contribute to department strategy and objectives as a member of the CORE team and represent HE&OR on key initiatives.
- Support pipeline assets as needed.
- Graduate degree (PhD or masters) and/or relevant work experience in health economics, outcomes research, epidemiology, health services research, public health, or health policy.
- 5+ years in the pharmaceutical industry or a managed care setting in the direct conduct of health economics, outcomes research, real‑world evidence, and epidemiology studies.
- Prior experience with outcomes research methods, including study design and analysis.
- Economic modeling experience is strongly preferred.
- Demonstrated research accomplishments evidenced by a history of peer‑reviewed publications.
- Experience working with HTA process in key markets in a market access environment required.
For US based candidates, the proposed salary band for this position is $ – $.
Benefits- 401(k) Plan: 100% match on the first 6% of contributions.
- Health benefits:
Two medical plan options (including HDHP with HSA), dental, and vision insurance. - Voluntary plans:
Critical illness, accident, and hospital indemnity insurance. - Time off:
Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave. - Support resources:
Access to child and adult backup care, family support programs, financial wellness tools, and emotional well‑being support. - Additional perks:
Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses.
Further details on eligibility for compensation and benefits based on role will be provided during the recruitment process.
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Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed‑term employment contract for a year. If the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed‑term employment contract.
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