Medical Director
Genmab
August 09, 2026
Remote friendly (Princeton, NJ)
United States
Medical Affairs
The Role
We are looking for an experienced and dedicated Medical Director to be a part of our Global Clinical Development Team.
Medical Director accountability includes medical oversight of one or more clinical trials, medical review and communication of data, and 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, clinical/regulatory documents, annual safety updates, and registration dossiers (e.g., protocol, ICF, IB, study reports, IND/clinical dossiers).
- Oversee early-stage programs; 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 potential new projects (internal & external).
- Contribute to publication and clinical communication strategy; provide inputs to external presentations.
- Provide strategic input and development support for clinical plans and individual trial protocols.
- Interact with key opinion leaders to implement latest clinical/medical thinking into development plans and consider novel methods/new targets.
- Contribute to medical best practices, standardization, and cross-functional process improvements.
- Support case report forms, medical monitoring, investigator/site liaison, preliminary/exploratory analyses, author clinical study reports, and participate in advisory boards.
- Serve as medical/technical resource for clinical issues from collaborators, investigators, consultants, and contractors.
- Create medical deliverables (clinical development plans, concept sheets, briefing books, label/marketing application dossier).
- Contribute to medical input for preclinical development of candidate therapeutic antibodies.
- Drive and monitor quality of clinical documents produced by CDT; attend relevant congresses.
Requirements
- MD degree.
- 3+ years of oncology clinical development experience, including leading/supporting Phase 3 studies.
- Oncology clinical experience required; solid tumor experience preferred.
- Proven ability to build/lead teams and inspire trust; represent organization internally/externally.
- Experience training/managing team members.
Benefits (US based, full-time within first year; eligibility may vary)
- 401(k): 100% match on first 6%.
- Health benefits (two medical options, dental, vision), voluntary plans.
- Paid time off and 12 weeks discretionary paid parental leave.
- Support resources (backup care, family support, financial wellness tools, emotional well-being support).
- Commuter benefits, tuition reimbursement, Lifestyle Spending Account.
Compensation (US based)
- Proposed salary band: $202,800.00–$304,200.00.
No application instructions provided.
We are looking for an experienced and dedicated Medical Director to be a part of our Global Clinical Development Team.
Medical Director accountability includes medical oversight of one or more clinical trials, medical review and communication of data, and 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, clinical/regulatory documents, annual safety updates, and registration dossiers (e.g., protocol, ICF, IB, study reports, IND/clinical dossiers).
- Oversee early-stage programs; 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 potential new projects (internal & external).
- Contribute to publication and clinical communication strategy; provide inputs to external presentations.
- Provide strategic input and development support for clinical plans and individual trial protocols.
- Interact with key opinion leaders to implement latest clinical/medical thinking into development plans and consider novel methods/new targets.
- Contribute to medical best practices, standardization, and cross-functional process improvements.
- Support case report forms, medical monitoring, investigator/site liaison, preliminary/exploratory analyses, author clinical study reports, and participate in advisory boards.
- Serve as medical/technical resource for clinical issues from collaborators, investigators, consultants, and contractors.
- Create medical deliverables (clinical development plans, concept sheets, briefing books, label/marketing application dossier).
- Contribute to medical input for preclinical development of candidate therapeutic antibodies.
- Drive and monitor quality of clinical documents produced by CDT; attend relevant congresses.
Requirements
- MD degree.
- 3+ years of oncology clinical development experience, including leading/supporting Phase 3 studies.
- Oncology clinical experience required; solid tumor experience preferred.
- Proven ability to build/lead teams and inspire trust; represent organization internally/externally.
- Experience training/managing team members.
Benefits (US based, full-time within first year; eligibility may vary)
- 401(k): 100% match on first 6%.
- Health benefits (two medical options, dental, vision), voluntary plans.
- Paid time off and 12 weeks discretionary paid parental leave.
- Support resources (backup care, family support, financial wellness tools, emotional well-being support).
- Commuter benefits, tuition reimbursement, Lifestyle Spending Account.
Compensation (US based)
- Proposed salary band: $202,800.00–$304,200.00.
No application instructions provided.