Associate Medical Director

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

The Role

We are looking for an experienced and dedicated Associate Medical Director to be a part of our team. The Associate Medical Director will contribute to the development of the program strategy for assigned trials/compounds and participate in the development of the clinical development plan, support/lead creation/review of clinical components of key documents, clinical and regulatory documents, annual safety updates, and registration dossiers for registration, market access, and commercialization of the compound(s). Oversee and develop clinical component projects including component studies.

Responsibilities

• Contribute to the development of the program strategy for assigned trials/compounds and participate in the development of the clinical development plan (CDP)
• Support/lead creation/review of clinical components of key documents, clinical and regulatory documents, annual safety updates, and registration dossiers (ie, protocol, ICF, IB, annual safety updates, study reports, regulatory submissions [Briefing documents, IND, Clinical dossiers] for registration, market access, and commercialization of the compound(s)
• Oversee and develop clinical component projects including component studies, with guidance from (Sr.) Medical Director as appropriate
• Support oversight of the safety of the drug, including the safety aspects of patients in clinical studies and signal detection
• Support creation, integration, and execution of overall medical strategy of assigned clinical development programs
• Contribute to publication and clinical communication strategy in coordination with Scientific Communications; provide inputs to key external presentations
• Provide strategic input and development support for clinical plans and individual trial protocols.
• Support interaction with key opinion leaders to ensure implementation of the latest clinical and medical thinking and guidelines into clinical development plans, as well as consideration of novel medical methods development and new potential targets
• Support the development of case report forms, perform medical monitoring, liaise with investigators, and site personnel, perform preliminary and exploratory data analyses on clinical trials, author clinical study reports, provide input on publication materials, and participate in advisory boards
• Contribute to medical input to preclinical development of candidate therapeutic antibodies
• Drive and monitor quality of all clinical documents (e.g., Investigators’ Brochures, protocols, study reports, clinical components of regulatory submissions, safety documents) produced by CDT, , with guidance from (Sr.) Medical Director as appropriate
• Participate in multi-function teams necessary for the advancement of the product pipeline
• Attend relevant congresses or other relevant forum to maintain up-to-date scientific/medical knowledge

Qualifications

• MD background with a minimum of 2+ years of directly related industry experience (or medical specialty clinical practice) within oncology or hematology
• Experience representing team and organization in a variety of internal/external settings
• Scientific background and/or deep understanding of immuno-oncology and or clinical care of oncology patients  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.

About You

• You are genuinely passionate about our purpose

• You bring precision and excellence to all that you do

• You believe in our rooted-in-science approach to problem-solving

• You are a generous collaborator who can work in teams with a broad spectrum of backgrounds

• You take pride in enabling the best work of others on the team

• You can grapple with the unknown and be innovative

• You have experience working in a fast-growing, dynamic company (or a strong desire to)

• You work hard and are not afraid to have a little fun while you do so!

Locations

Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.

About Genmab

Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines.

Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X .

Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com) .

Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the contract.