Associate Director, Health Evidence and Outcomes Liaison (Northeast)

Genmab • Newark, NY

20h • Remote

About The Position

Genmab is seeking a Regional field-based Health Evidence and Outcomes Liaison (HEOL) to join its U.S. Medical Affairs team. This role is part of a passionate, high-profile, high-impact team working in a dynamic and collaborative setting. The HEOL team is Genmab’s field-based Medical Affairs function, responsible for establishing access and operational success across payor organizations. They collaborate closely with Genmab’s in-house CORE team (Center for Observational Research, Real-world Evidence and Epidemiology) and the US Market Access team. The Regional HEOL will communicate clinical, humanistic, Real World Evidence (RWE), and health economic (HCEI) data to support Genmab products throughout their lifecycle. HEOLs engage in scientific exchange with Population Health Decision Makers (PHDMs) in a fair and balanced manner, proactively communicating the clinical/economic value of Genmab’s pipeline in accordance with FDAMA 114 and the 21st Century Cures Act. This role will cover the entirety of the Genmab portfolio where U.S. Market Access support is assigned to Genmab. Domestic travel of over 50% will be required. This is a remote position covering the Northeastern United States, and the incumbent must reside within the assigned geography.

Requirements

• Advanced/scientific medical degree strongly preferred (PharmD, PhD, MD, MPH, MS, etc.).
• At least 5 years of field HEOR or Value Liaison experience generating and/or communicating meaningful evidence to US payers and population health decision-makers is required.
• Experience in the hematology/oncology space; expertise in lymphoma, leukemia, thoracic, and gynecological oncology experience a plus.
• Strong knowledge of the US healthcare, payer, and market access environments.
• Advanced understanding of operational support for buy-and-bill products.
• Expert technical knowledge of HEOR, including the use of RWE, data analytics, and economic modeling.
• Proven ability to work independently, as well as cross-functionally with several internal stakeholders in a high-matrixed environment, including joint venture collaborations.
• Preferred experience on product launches or demonstrated success as a product or therapeutic point to PHDMs.
• Excellent interpersonal communication and presentation skills, strong personal integrity, teamwork abilities, and a customer focus are necessary.
• Must be able to organize, prioritize, and work effectively in a constantly changing environment.
• Strong compliance knowledge of and adherence to corporate compliance policies.
• Current working knowledge of FDAMA 114, 21st Century Cures Act, HIPAA, and other compliance regulations and guidelines relevant to industry interactions with payers and population health decision-makers.
• Demonstrated technical acumen including MS Office skills, Veeva PromoMats, and the ability to adapt and leverage multiple business applications.

Nice To Haves

• expertise in lymphoma, leukemia, thoracic, and gynecological oncology experience a plus.

Responsibilities

• Have a deep scientific knowledge of Genmab’s products and pipeline, their target disease areas, and the competitive landscape.
• Build and maintain a strategic engagement plan with key payor accounts in assigned geographies.
• Work in close coordination with National HEOLs to ensure alignment of strategy and tactics seamlessly flow from National to Regional accounts (ex. GPO >>> LPG).
• Identify key accounts and RWE experts that align with CORE AOIs and appropriately liaise opportunities and ongoing CORE studies to internal leads.
• Understand the access landscape including regional payer policies and pathways in respective therapeutic areas.
• In close collaboration with the US Market Access team, execute engagement strategy for key payer customers (regional payers, health systems, large practice groups (LPGs)/community networks, and regional strategic partners) for compliant delivery of pre-approval information exchange (PIE), HCEI, RWE, and clinical materials.
• Be fluent in HCEI and clinical content prepared by CORE for engagements with PHDMs at local/regional payor accounts.
• Provide medical and HCEI leadership supporting the access and operationalization of Genmab therapies across health systems.
• Provide clinical, humanistic, and HCEI education relative to target disease states and Genmab clinical trials to payers and PHDMs.
• Present appropriate economic and clinical information to PHDMs in response to unsolicited requests (as appropriate) in a fair and balanced manner.
• Develop and establish relationships with key PHDMs and bring forth appropriate collaboration opportunities that meet USMA and Genmab goals and objectives.
• Provide insights/feedback to internal CORE and Medical Strategy team members on emerging economic/clinical and real-world data that enhance the value and appropriate use of Genmab products.
• Collaborate effectively and proactively establish working relationships with cross-functional teams including internal CORE, US Medical Affairs, Field Medical Affairs (FMA), and Market Access.
• Professionally represent Genmab at select medical and scientific conferences including providing scientific coverage and competitive intelligence.

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

What This Job Offers

• Job Type: Full-time
• Career Level: Director
• Number of Employees: 501-1,000 employees