Medical Director

Genmab is an international biotechnology company focused on antibody therapeutics, dedicated to improving patient lives through innovative and differentiated products.

We are looking for an experienced and dedicated Medical Director to be a part of our Global Clinical Development Team.

• Lead development of program strategy for assigned trials/compounds and participate in the development of the clinical development plan (CDP).
• Lead creation and review of clinical components of key documents, regulatory submissions, and registration dossiers.
• Oversee early‑stage programs and develop clinical programs, including component studies.
• Oversee safety of the drug, including patient safety in clinical studies and signal detection with support of the Safety physician.
• Create, integrate, and execute overall medical strategies of assigned clinical development programs; provide strategic medical advice on potential new projects.
• Contribute to publication and clinical communication strategy in coordination with Scientific Communications; provide inputs to key external presentations.
• Provide strategic input and development support for clinical plans and individual trial protocols.
• Interact with key opinion leaders to incorporate latest clinical and medical guidelines into development plans.
• Contribute to medical department best practices, standardization, and cross‑functional process improvements.
• Support the development of case report forms, perform medical monitoring, liaise with investigators, and conduct preliminary data analyses.
• Support development of other relevant documents necessary for product pipeline advancement.
• Serve as medical and technical resource for clinical issues raised by collaborators, investigators, consultants, and contractors.
• Create medical deliverables such as clinical development plans, concept sheets, briefing books, and labeling dossiers.
• Contribute medical input to preclinical development of candidate therapeutic antibodies.
• Drive and monitor quality of all clinical documents produced by CDT.
• Participate in multi‑function teams essential to product pipeline advancement.
• Attend relevant congresses or forums to maintain up‑to‑date scientific and medical knowledge.

• MD degree.
• Minimum of 3+ years of directly related industry experience in oncology clinical development, including Phase 3 clinical studies.
• Clinical experience in oncology required; experience in solid tumors preferred.
• Proven ability to build and lead teams and inspire trust among colleagues.
• Experience representing team and organization in internal and external settings.
• Experience training and managing team members.
• Proven performance in earlier or comparable role.

For U.S. based candidates, the proposed salary band is $—$. The actual offer will consider skill set, experience, and location and may include discretionary bonuses and long‑term incentives.

• 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.

• Genuinely passionate about our purpose.
• Brings precision and excellence to all tasks.
• Believes in a rooted‑in‑science approach to problem‑solving.
• An open collaborator who works well in diverse teams.
• Prides in enabling the best work of others on the team.
• Innovative and capable of grappling with the unknown.
• Has experience in a fast‑growing, dynamic company, or a strong desire to.
• Hard work and a willingness to have fun while doing so.

Genmab is an agile, hybrid organization with offices worldwide. Candidates may work remotely or in one of our community‑based office spaces designed to foster collaboration.