This job has expired

(Associate) Medical Director

Princeton, NJ
Genmab covers entire cost of medical benefit premiums
Closing date
Jun 11, 2023

View more

Medical Director
Full Time

Job Details

At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.


The Role:


We are looking for an experienced and dedicated Associate Medical Director or Medical Director (depending on experience) to be a part of our Global Clinical Development Team. 


The (Assoc.) Medical Director will be accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents and presentations.



  • Directing study design, protocol development and execution of clinical research for pivotal cancer studies.

  • Contributing to the overall medical strategy of the assigned clinical development programs and product pipeline as well as giving in-depth medical advice on potential new projects (internal and external).

  • Generating/reviewing clinical components of key documents (regulatory documents, registration dossiers, value dossiers, pharmacoeconomic dossiers) supporting registration, market access and commercialization of the compound(s).

  • Ensuring quality of all clinical documents (e.g. Investigators’ Brochure, protocols, study reports, clinical components of regulatory submissions, safety related documents).

  • Also, the Employee shall act as medical expert and have the ability to lead interactions with external stakeholders (e.g. regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups) internal stakeholders (e.g. Research, Translation Medicine, Safety, Regulatory, Global Medical Affairs and Commercial) and internal decision boards.


Moreover, the Employee shall:

  • Oversee the safety aspects of patients in clinical studies and signal detection with support of the Safety physician.

  • Plan and execute publication and clinical communication strategy in coordination with Scientific Communications.

  • Provide input to key external presentations.

  • Ensure career development of functional reports (esp. clinical research scientists) and other CMT colleagues through active participation in the performance management and talent planning processes.

  • Provide on-boarding, training and mentoring support and contribute to the performance evaluation of CMT members as appropriate.

  • The Employee shall also render such other related services and duties as may be assigned from time to time by supervisor.

  • Participate in interviews of new potential hires for the Medical Department.

  • Act as the Study Lead and, when needed, represent the program or disease area.

  • Be proactive in interacting with the different line functions to ensure alignment with the objectives of the Medical Department.



  • MD background with 3- 5 years industry experience.

  • Training in Oncology is strongly preferred.

  • Experience as a responsible Medical Officer for clinical trial(s) is required.

  • Scientific background and/or deep understanding of solid tumor oncology is strongly preferred.

  • Ability to represent the Company in a variety of internal and external settings.

  • Persuasive and effective in personal interactions at all levels of the organization.

  • Demonstrated success in teamwork within a matrix organization and ability to inspire trust among colleagues.

  • Innovative, flexible, resilient and visionary with the ability to seize opportunities.

  • Ability to prioritize, respond to directives, and work in a fast-paced and changing environment.

  • Result and goal-oriented and committed to contributing to the overall success of Genmab.

  • Deep desire to make a difference.


Be part of the extra[not]ordinary™

Are you caring, candid, impact-driven and determined to make a difference? Join our unstoppable team as we improve the lives of patients through innovative and differentiated antibody therapeutics.

About Genmab

Founded in 1999 in Copenhagen, Denmark, Genmab is an innovative biotech company that has become a leader in antibody biology and innovation. Our product pipeline and next-generation antibody technologies are the result of our strong company culture, a deep passion for innovation, and desire to transform cancer treatment and serious diseases.

When you work with us, you’ll be part of a warm, fun, dynamic community, and team up with some of the best, most authentic individuals in locations around the world, who care deeply and share in a relentless drive to innovate and create transformational medicines. People who are candid, impact-driven, and a little unconventional; who seek out and embrace the opportunity to build new and bold futures within a rapidly growing and innovative biotech company; who bring their full selves to work and show up for each other - rolling up their sleeves to get the job done. This translates into a place where you can be authentically you; are empowered to innovate, build solutions, and execute; feel cared for and supported in growth; and are a critical part of changing the lives of patients around the world through transformative cancer treatment.

Find Us

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert