Associate Director, Medical Communications and Publications, CORE Publications

Genmab•Plainsboro Township, NJ

1d•$162,640 - $243,960•Hybrid

About The Position

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 Associate Director of Medical Communications and Publications will be responsible for leading the strategic planning, development, and execution of Health Economics and Outcomes Research (HEOR) publication plans across one or more therapeutic areas. The individual will collaborate with members of the Center for Outcomes Research, Real World Evidence and Epidemiology (CORE) to drive the development of publication strategy, planning, and execution of high-quality scientific publications. The individual will also collaborate cross-functionally with Medical Affairs, Market Access, Clinical Development, Biostatistics, and external experts to translate data into impactful publications aligned with the global value strategy. Functioning as a member of the Global Medical Affairs department, this individual will report to the Sr Director of Medical Communications and Publications. Work arrangement: This role offers flexibility to work away from the office for 20%–40% of a typical schedule. Employees may use this work schedule in increments of single days or multiple consecutive days, provided it does not exceed 40% within a 60-day period, and is approved by the hiring manager.

Requirements

Advanced degree: PharmD, PhD, DrPH or MPH required. Certification as a Medical Publication Professional (CMPP) desirable.
Knowledge of HEOR/RWE publications and strong understanding of economic modeling, RWE, epidemiological and PRO research
5+ years in medical publications, experience in HEOR, value evidence or related field within the pharmaceutical or biotech industry.
Experience across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization process.
Ability to drive and execute within a large matrix, cross-functional team, and work successfully in a fast-paced environment.
Proven ability to think strategically at an enterprise level and make decisions even under conditions of ambiguity, evolving landscapes, fast paced, and tight timelines.
In-depth understanding of good publication practices and guidance (GPP, ICMJE), and other guidance related to scientific data communication.
Ability to travel domestically and internationally approximately 20% of time.

Responsibilities

Develop and lead comprehensive global/regional publication strategies and initiatives including abstracts, congress presentations, and manuscripts for assigned assets/therapeutic areas and provide expertise to the matrix team in developing and executing the medical communication plan.
In development of a strategic publication plan, the individual will 1) collaborate with cross-functional, key global stakeholders 2) anticipate gaps and identify solutions for publication planning people 3) recognize changes in the healthcare and treatment landscape and adjust publication/communication plans in a timely and efficient manner 4) ensure alignment with broader medical and CORE publication strategies.
Serve as a therapy area and product expert for both internal and external stakeholders.
Develop scientific content (including PLS, FAQs) in collaboration with key stakeholders, ensuring development of materials that address requests from health care providers and payers.
Serve as the subject matter expert on publication-related matters establishing strong working closely with both internal and external disease-area experts to ensure high quality analysis, interpretation, communication, and publication planning of data.
Collaborate effectively with cross functional colleagues and key stakeholders across cultures, backgrounds, and geographies.
Manage annual budget and work within allocated resources, ensuring contracts, SOWs and invoices are submitted accurately and in a timely manner to ensure high quality deliverables.
Liaise with agency/vendor partners to ensure timely delivery of quality publication by providing direction, reviewing developed content, and ensuring process is consistent with Genmab SOPs.
Bring subject matter expertise in discussions regarding the creation or updates to departmental SOPs improving/modifying processes and procedures helping to achieve organizational goals.

Benefits

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

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