Medical Director
Genmab
August 07, 2026
Remote friendly (Princeton, NJ)
United States
Medical Affairs
The Role
- Medical oversight of one or more clinical trials, medical review/communication of data, and medical input into regulatory documents and presentations.
Responsibilities
- Direct study design, protocol development, and execution of clinical research for pivotal cancer studies.
- Contribute to medical strategy for assigned clinical development programs and product pipeline; provide in-depth medical advice on potential new projects (internal/external).
- Generate/review clinical components of key documents (regulatory documents, registration dossiers, value dossiers, pharmacoeconomic dossiers) supporting registration, market access, and commercialization.
- Ensure quality of clinical documents (e.g., Investigators’ Brochure, protocols, study reports, clinical components of regulatory submissions, safety-related documents).
- Act as medical expert and lead interactions with external stakeholders (e.g., regulatory authorities, KOLs, advisory boards, patient advocacy groups) and internal stakeholders (e.g., Research, Translation Medicine, Safety, Regulatory, Global Medical Affairs, Commercial) and internal decision boards.
Moreover, The Employee Shall
- Oversee patient safety aspects in clinical studies and signal detection (with support of Safety physician).
- Plan/execute publication and clinical communication strategy (with Scientific Communications).
- Provide input to key external presentations.
- Support career development, onboarding/training/mentoring, and performance evaluation of CMT colleagues.
- Perform other related duties as assigned; participate in interviews of potential hires.
- Act as Study Lead and represent program/disease area when needed; align with Medical Department objectives.
Requirements
- MD; minimum 3 years direct industry experience in oncology or hematology.
- Experience as responsible Medical Officer for clinical trials.
- Solid tumor oncology understanding strongly preferred.
- Ability to represent the company internally/externally; persuasive interpersonal skills.
- Proven teamwork in matrix organizations; innovative, flexible, resilient, visionary.
- Ability to prioritize in fast-paced environments; result/goal-oriented; deep desire to make a difference.
- Medical oversight of one or more clinical trials, medical review/communication of data, and medical input into regulatory documents and presentations.
Responsibilities
- Direct study design, protocol development, and execution of clinical research for pivotal cancer studies.
- Contribute to medical strategy for assigned clinical development programs and product pipeline; provide in-depth medical advice on potential new projects (internal/external).
- Generate/review clinical components of key documents (regulatory documents, registration dossiers, value dossiers, pharmacoeconomic dossiers) supporting registration, market access, and commercialization.
- Ensure quality of clinical documents (e.g., Investigators’ Brochure, protocols, study reports, clinical components of regulatory submissions, safety-related documents).
- Act as medical expert and lead interactions with external stakeholders (e.g., regulatory authorities, KOLs, advisory boards, patient advocacy groups) and internal stakeholders (e.g., Research, Translation Medicine, Safety, Regulatory, Global Medical Affairs, Commercial) and internal decision boards.
Moreover, The Employee Shall
- Oversee patient safety aspects in clinical studies and signal detection (with support of Safety physician).
- Plan/execute publication and clinical communication strategy (with Scientific Communications).
- Provide input to key external presentations.
- Support career development, onboarding/training/mentoring, and performance evaluation of CMT colleagues.
- Perform other related duties as assigned; participate in interviews of potential hires.
- Act as Study Lead and represent program/disease area when needed; align with Medical Department objectives.
Requirements
- MD; minimum 3 years direct industry experience in oncology or hematology.
- Experience as responsible Medical Officer for clinical trials.
- Solid tumor oncology understanding strongly preferred.
- Ability to represent the company internally/externally; persuasive interpersonal skills.
- Proven teamwork in matrix organizations; innovative, flexible, resilient, visionary.
- Ability to prioritize in fast-paced environments; result/goal-oriented; deep desire to make a difference.