Vice President, Program Medical Lead
Genmab
June 27, 2026
Remote friendly (Boston, MA)
United States
Clinical Research and Development
The Role
- Oversee Genmab’s pivotal/registrational Clinical Development program(s) in oncology; act as medical expert with Health Authorities.
- Provide managerial oversight for physicians on assigned programs.
- Lead end-to-end medical input and execution of clinical strategy for specified projects.
- Create medical deliverables: clinical development plans, concept sheets, briefing books, and label/marketing application dossiers.
- Provide input to intellectual property strategy by translating organizational strategy into clinical strategy.
- Support business development/alliance management with medical input for candidate in-licensing and collaboration/due diligence/investor activities.
- Serve as Responsible Medical Officer for programs under oversight.
- Oversee/develop clinical projects including component studies; provide strategic input for clinical plans and study protocols.
- Provide medical/clinical/scientific leadership to ongoing studies and development options; contribute to identification/validation of new molecular targets and disease indications.
- Provide hematology/oncology medical expertise, including competitor knowledge.
- Contribute to safety surveillance (supervisory) and represent Medical function in Safety Committees; be on CRO alert list.
- Participate ad hoc in strategic initiatives, coordinating medical input for preclinical development.
- Support regulatory/ICH-GCP/business development documentation and advance pipeline via multi-functional teams and governance fora.
- Build relationships with internal departments and medical/scientific community; serve as resource for clinical issues.
- Collaborate cross-functionally at congresses; incorporate latest clinical/medical thinking into development plans.
Requirements
- MD/MBChB (accredited institution) and board-certified specialist qualification (or equivalent).
- >15 years clinical/academic/industry leadership; >10 years oncology clinical trials.
- Strong clinical trial data analysis and synthesis for scientific disclosure.
- Experience preparing NDA/BLA filings in hematology/oncology (FDA, EMA/CHMP, PMDA, MHRA).
- Expertise in scientific/medical/commercial development of innovative product platforms.
- Strong written/verbal communicator.
- ~20% travel.
- Office-based/Hybrid in Boston, MA.
Benefits (US-based, within first year)
- 401(k) 100% match on first 6%.
- Two medical options (incl. HDHP with HSA), dental, vision.
- Critical illness, accident, hospital indemnity.
- Paid vacation/sick leave/holidays; 12 weeks discretionary paid parental leave.
- Backup care, family support, financial wellness tools, emotional well-being support.
- Commuter benefits, tuition reimbursement, Lifestyle Spending Account.
Application instructions
- Apply for the position via Genmab’s website.
- Oversee Genmab’s pivotal/registrational Clinical Development program(s) in oncology; act as medical expert with Health Authorities.
- Provide managerial oversight for physicians on assigned programs.
- Lead end-to-end medical input and execution of clinical strategy for specified projects.
- Create medical deliverables: clinical development plans, concept sheets, briefing books, and label/marketing application dossiers.
- Provide input to intellectual property strategy by translating organizational strategy into clinical strategy.
- Support business development/alliance management with medical input for candidate in-licensing and collaboration/due diligence/investor activities.
- Serve as Responsible Medical Officer for programs under oversight.
- Oversee/develop clinical projects including component studies; provide strategic input for clinical plans and study protocols.
- Provide medical/clinical/scientific leadership to ongoing studies and development options; contribute to identification/validation of new molecular targets and disease indications.
- Provide hematology/oncology medical expertise, including competitor knowledge.
- Contribute to safety surveillance (supervisory) and represent Medical function in Safety Committees; be on CRO alert list.
- Participate ad hoc in strategic initiatives, coordinating medical input for preclinical development.
- Support regulatory/ICH-GCP/business development documentation and advance pipeline via multi-functional teams and governance fora.
- Build relationships with internal departments and medical/scientific community; serve as resource for clinical issues.
- Collaborate cross-functionally at congresses; incorporate latest clinical/medical thinking into development plans.
Requirements
- MD/MBChB (accredited institution) and board-certified specialist qualification (or equivalent).
- >15 years clinical/academic/industry leadership; >10 years oncology clinical trials.
- Strong clinical trial data analysis and synthesis for scientific disclosure.
- Experience preparing NDA/BLA filings in hematology/oncology (FDA, EMA/CHMP, PMDA, MHRA).
- Expertise in scientific/medical/commercial development of innovative product platforms.
- Strong written/verbal communicator.
- ~20% travel.
- Office-based/Hybrid in Boston, MA.
Benefits (US-based, within first year)
- 401(k) 100% match on first 6%.
- Two medical options (incl. HDHP with HSA), dental, vision.
- Critical illness, accident, hospital indemnity.
- Paid vacation/sick leave/holidays; 12 weeks discretionary paid parental leave.
- Backup care, family support, financial wellness tools, emotional well-being support.
- Commuter benefits, tuition reimbursement, Lifestyle Spending Account.
Application instructions
- Apply for the position via Genmab’s website.