Medical Director – Oncology Clinical Development (Remote)

Genmab; Utrecht; Hybrid; EUR 188,697 - 255,297; Full time

Job summary

Genmab is seeking a Medical Director to oversee medical aspects of clinical trials, review data, and contribute to regulatory documents for antibody therapeutics. This role entails leading program strategies, drafting clinical and regulatory materials, and guiding cross‑functional teams in an international setting.

You will provide strategic medical input on trial design, publication strategy, and advisory boards, while ensuring alignment with safety and regulatory requirements.

Qualifications

• MD degree.
• 3+ years of oncology clinical development experience, including Phase 3 leadership/support.
• Clinical oncology experience; solid tumors preferred.
• Proven ability to build and lead teams and inspire trust.
• Experience representing team in internal/external settings.
• Experience training and managing team members.
• Proven performance in earlier or comparable role.

Responsibilities

• Lead development of program strategy for assigned trials/compounds and contribute to the CDP.
• Lead creation and review of clinical and regulatory documents supporting submissions.
• Oversee early-stage programs and develop clinical programs including component studies.
• Oversee safety of the drug and signal detection with support of Safety physician.
• Create and execute strategic medical plans for development programs.

Skills

Team leadership

Cross-functional collaboration

Mentoring

Stakeholder management

Education

MD degree

Job description

Genmab is seeking a Medical Director to oversee medical aspects of clinical trials, review data, and contribute to regulatory documents for antibody therapeutics. This role entails leading program strategies, drafting clinical and regulatory materials, and guiding cross‑functional teams in an international setting.

You will provide strategic medical input on trial design, publication strategy, and advisory boards, while ensuring alignment with safety and regulatory requirements.