Medical Director
Genmab
August 30, 2026
Remote friendly (Princeton, NJ)
United States
Medical Affairs
The Role
We are looking for an experienced and dedicated Medical Director to be part of our Global Clinical Development Team. The Medical Director will provide medical oversight of one or more clinical trials, review and communicate data, and provide medical input into regulatory documents and presentations.
Responsibilities
- Lead program strategy for assigned trials/compounds and participate in development of the clinical development plan (CDP).
- Lead creation and review of clinical components of key documents and regulatory dossiers (protocol, ICF, Investigator’s Brochure, annual safety updates, study reports, regulatory submissions such as briefing documents/IND/clinical dossiers).
- Oversee early-stage programs and develop clinical programs including component studies.
- Oversee drug safety, including patient safety in clinical studies and signal detection (with support of the Safety physician).
- Create, integrate, and execute medical strategies; provide strategic medical advice on new projects (internal/external).
- Coordinate clinical communication and publications; provide inputs to key external presentations.
- Provide development support for clinical plans and individual trial protocols.
- Engage key opinion leaders to incorporate latest clinical/medical thinking and guidelines.
- Contribute to medical best practices, standardization, and cross-functional process improvements.
- Support case report forms, medical monitoring, investigator/site liaison, data analyses, clinical study reports, publication inputs, and advisory boards.
- Create medical deliverables (clinical development plans, concept sheets, briefing books, label/marketing application dossier).
- Drive and monitor quality of clinical documents produced by CDT.
- Attend relevant congresses to maintain up-to-date knowledge.
Requirements
- MD degree.
- 3+ years oncology clinical development experience, including leading/supporting Phase 3 studies.
- Oncology clinical experience required; solid tumor experience preferred.
- Proven ability to build/lead teams; represent organization internally/externally.
- Experience training/managing team members.
- Proven performance in earlier/comparable role.
Application instructions
Does this inspire you and feel like a fit? Then we would love to have you join us!
We are looking for an experienced and dedicated Medical Director to be part of our Global Clinical Development Team. The Medical Director will provide medical oversight of one or more clinical trials, review and communicate data, and provide medical input into regulatory documents and presentations.
Responsibilities
- Lead program strategy for assigned trials/compounds and participate in development of the clinical development plan (CDP).
- Lead creation and review of clinical components of key documents and regulatory dossiers (protocol, ICF, Investigator’s Brochure, annual safety updates, study reports, regulatory submissions such as briefing documents/IND/clinical dossiers).
- Oversee early-stage programs and develop clinical programs including component studies.
- Oversee drug safety, including patient safety in clinical studies and signal detection (with support of the Safety physician).
- Create, integrate, and execute medical strategies; provide strategic medical advice on new projects (internal/external).
- Coordinate clinical communication and publications; provide inputs to key external presentations.
- Provide development support for clinical plans and individual trial protocols.
- Engage key opinion leaders to incorporate latest clinical/medical thinking and guidelines.
- Contribute to medical best practices, standardization, and cross-functional process improvements.
- Support case report forms, medical monitoring, investigator/site liaison, data analyses, clinical study reports, publication inputs, and advisory boards.
- Create medical deliverables (clinical development plans, concept sheets, briefing books, label/marketing application dossier).
- Drive and monitor quality of clinical documents produced by CDT.
- Attend relevant congresses to maintain up-to-date knowledge.
Requirements
- MD degree.
- 3+ years oncology clinical development experience, including leading/supporting Phase 3 studies.
- Oncology clinical experience required; solid tumor experience preferred.
- Proven ability to build/lead teams; represent organization internally/externally.
- Experience training/managing team members.
- Proven performance in earlier/comparable role.
Application instructions
Does this inspire you and feel like a fit? Then we would love to have you join us!