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.
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The Role
Reporting to the Director, Global Medical Affairs Strategy, the Associate Director will be the subject matter expert responsible for providing medical support to the development and execution of the Global Medical Affairs strategic and tactical plans and support the Global medical launch planning, and execution for gynecology oncology assets in close alignment and collaboration with the global medical strategy director.
As an integral part of the Global Medical Affairs Team, and in close collaboration with the medical affairs strategy team and cross-functional partners, the Global Medical Affairs Associate Director should have strong commercial aptitude and/or experience, including proven ability to translate and align commercial and scientific goals and objectives into actions. He/she will advise on the development of medical education and publication/communication tactics and support the learning and development of internal stakeholders. He/she will also support data generation and life cycle management initiatives as well as establish and maintain the relationships with the Global Key Opinion Leaders.
Responsibilities
- Support the execution of the Global medical affairs strategy and tactics for Genmab assets in Solid Tumor portfolio
- High quality scientific/clinical input and review of: Disease Strategy/plans, Commercial Brand plans and Integrated Evidence plans, abstracts, posters, slides, manuscripts in disease area, educational materials in disease area including slides, webcasts, etc., IST protocols in disease area, steering committee and advisory board meeting objectives and materials, booth panels, Med info letters, and promotional materials
- Provide medical oversight for company sponsored Medical Affairs led interventional and observational clinical trials
- Support cross-functional pre-launch/launch activities
- Prepare and give presentations for internal training and to external audiences
- Serve as a medical and content expert for internal and external stakeholders
- Play an integral role in the planning and execution of Global advisory boards and other Key Opinion Leader meetings
- Represent Genmab at key Global medical conferences/meetings
- Provide input for Medical and Promotional Review Committees
- Provide scientific/medical input into local regulatory/reimbursement/policy related documents and interactions
- In close collaboration with Field Medical Affairs, contribute to the development of a disease area Engagement Plan, including engagement plans for congresses and professional meetings
- Provide support for Medical Affairs cross-functional working groups and Alliance partnerships
- Contribute to scientific review and interpretation of key competitive data presentation and provide key implications to Genmab products
- Assist and collaborate with Medical Affairs colleagues to track priority Medical Affairs tactics and performance to goals/budget within Global and Regional Disease Strategy plans
- Assist in publication planning, gap analyses, content creation, and key scientific statements in partnership with Scientific and Medical Communications
- Contribute and assist in developing and delivering relevant training and materials for the broader Medical Affairs teams, globally
- Assist in the planning and execution of Early Access Program, Medical Affairs Sponsored Trials (as needed), within appropriate standards for compliance, quality, timeliness, and budget
Requirements
- Advanced degree (MS, PhD, PharmD, MD) in medicine, molecular biology, genomics, cancer biology or other relevant life sciences area preferred.
- 5+years of relevant clinical, medical affairs or medical communication experience in Oncology (preferably within solid tumors (GU, skin cancers experience is preferred)
- Industry experience, ideally including recent experience of a successful pre-launch & launch within Oncology
- Ability to think strategically about the short- and long-term impacts within the oncology health care landscape
- Ability to lead collaboratively across various internal stakeholders and develop trusted partnerships
- A strong ability to interpret and articulate clinical/HEOR data and the oncology clinical development programs
- Good understanding of compliance and regulatory requirements for pharmaceutical Medical Affairs, R&D and Commercial work
- Fair knowledge of evidence-based medicine concepts, applied biostatistics and health economics are desirable
- Demonstrated organizational skills to manage multiple projects simultaneously
- Strong written and verbal communication skills (including presentation skills) along with excellent judgment and ability to work in a matrix team environment
- Ability to work globally across time zones and travel internationally to conferences and meetings, which will include occasional weekend travel
For US based candidates, the proposed salary band for this position is as follows:
$150,080.00 - $225,120.00
The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.
When you join Genmab, you're joining a culture that supports your physical, financial, social, and emotional wellness. Within the first year, regular full-time U.S. employees are eligible for:
- 401(k) Plan: 100% match on the first 6% of contributions
- Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
- Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
- Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
- Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
- Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses
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 fixed-term employment contract.