VP Medical - Solid Tumors

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

Genmab continues to grow, and we are now looking for a Vice President, Solid Tumors to join our Medical Team to support Genmab´s further expansion.

The VP will be accountable for the medical oversight of several clinical trials, medical review and communication of data, and medical input into regulatory documents and presentations.

We are looking to fill this position in Copenhagen as an onsite position. The position reports to the Program Medical Head.

Responsibilities

• Translate organizational strategy into clinical strategies
• Accountable for the entire medical input, process, conception and execution of clinical strategy for specified projects
• Provide medical expertise in hematology and/or oncology, including relevant, up-to-date knowledge of competitor products
• Contribute in an active and ongoing manner to the scientific, medical and commercial development of current and future product candidates (internally and externally developed)
• Interact 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
• Act as medical expert in interactions with Health Authorities
• Establish productive, interactive relationships with relevant internal departments, as well as the medical and scientific community. Serve as medical and technical resource for clinical issues raised by internal and external collaborators, investigators, consultants and contractors
• Create medical deliverables: clinical development plans, concept sheets, briefing books, and label and marketing application dossier
• Contribute and coordinate medical input to preclinical development of candidate therapeutic antibodies
• Participate in selection of the right product candidates for clinical development, etc.
• Support business development activities as needed, including due diligence activities and investor activities
• Support business development and alliance management by providing medical input into the assessment of candidate in-licensing products and ensuring optimal collaboration with partners.
• May act as delegate to approve labeling documents.

Requirements

• It is required that you have an MD background with 10+ years industry experience and Medical Specialist leadership roles
• Training in Oncology
• Experience as a responsible Medical Officer for pivotal clinical trial(s) and Regulatory submissions/interactions with major Health Authorities 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

Moreover, it is expected that you are/have:

• 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

The proposed gross annual/hourly base salary range for this position, in the primary location, based on a full time schedule is:

DKK1.351.200,00-2.026.800,00

The final salary offer will depend on several factors, including your skills, qualifications, and experience.

In addition to base salary, this position is eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.

When you join Genmab, you become a part of a culture that supports your physical, financial, social, and emotional well-being. Our benefits include, but are not limited to:

• Pension
• Health insurance and wellness benefits
• Paid time off
• Employee support programs

Further details on eligibility for compensation and benefits based on the role will be provided during the recruitment process.

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.

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