Associate Director, Medical Information

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

In Medical Information, we will deliver high-quality medical and scientific information to healthcare professionals, patients and internal stakeholders. We serve as a therapy area and product experts for both internal and external customers, including the Medical Information Call Center. We conduct medical reviews to ensure accuracy and appropriateness.

As an Associate Director, you will contribute to Medical Information planning for new product launches, line extensions, and key data releases, as applicable. You will develop Field Medical resources to help educate on Genmab’s technologies and pipeline products. You will also proactively analyze customer inquiry data to identify trends and knowledge gaps; strategically communicates actionable insights to cross-functional stakeholders to inform business planning.

Domestic and international travel will be required, including approximately 2-3 domestic and international congresses and company meetings.

You will report to Senior Director, Head of Global Medical Information, based in the US. This role is located in Utrecht, the Netherlands.

Responsibilities

• Provide scientifically accurate, balanced, and timely responses to inquiries.

• Ensure all responses and materials align with European Medicines Agency (EMA), country-specific regulations, and industry codes of practice such as EFPIA (European Federation of Pharmaceutical Industries and Associations.

• Develop, localize and maintain high-quality, scientifically accurate and balanced medical and scientific information, including Standard/Custom Response Letters, FAQs and Field Medical resources.

• Collaborate with global teams to ensure medical information materials support local product-related inquiries.

• Train and serve as the escalation point for triage of complex inquiries from the European Medical Information Call Center.

• Provide medical information review of promotional materials to ensure content is accurate.

• Lead Medical Information planning for new product launches, line extensions, and key data releases, as applicable.

• Proactively analyze and distribute actionable insights and metrics to relevant functions to inform medical strategy.

• Represent Medical Information function at interdisciplinary meetings, congresses and vendor discussions.

Requirements

• Scientific or Medical Degree is required (MD, PhD or MSc in Medicine, Pharmacy, Biomedical Science).

• At least 7+ years of pharmaceutical industry-based Drug Information, Medical Writing or Medical/Promotional review experience.

• Prior experience in Oncology preferred.

• Excellent written and verbal communication skills, with the ability to convey complex scientific information clearly and concisely.

• Strong knowledge of European regulatory requirements (e.g., EMA, MHRA) and industry codes (e.g., EFPIA).

• Fluency in English is essential; additional European languages (e.g., French, German, Spanish, or Italian) are advantageous.

• Strong leadership and organization skills with a solutions orientated approach driving optimal business results in a complex matrix environment.

• Excellent written and verbal communication skills including presentation skills.

• Demonstrates flexibility in response to changing needs and competing demands.

About You

• You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment
• You bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solving
• You are a generous collaborator who can work in teams with diverse backgrounds
• You are determined to do and be your best and take pride in enabling the best work of others on the team
• You are not afraid to 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 leverages the effectiveness of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are designed as open, community-based spaces that work to connect employees while being immersed in our state-of-the-art laboratories. Whether you’re in one of our collaboratively designed 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 guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics. For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates. To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies. 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 locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S. and Tokyo, Japan. 
 

Our commitment to diversity, equity, and inclusion

We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, or genetic information. Learn more about our commitments on our website. 

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 fixed-term employment contract.