US Director, Payor & Access Strategy Lead, Medical Affairs, Health Systems
Job in
Dover, Kent County, Delaware, 19904, USA
Listed on 2026-07-13
Listing for:
Merck
Full Time
position Listed on 2026-07-13
Job specializations:
-
Healthcare
Healthcare Management, Healthcare Administration, Healthcare Consultant
Job Description & How to Apply Below
* ** Role Summary*
* + The US Director, Payor & Access Strategy Lead, Medical Affairs (PASL) is responsible for US Field Medical (FM) strategy, training, and prioritization of the Value & Implementation (V&I) plan for USMA Health Systems (HS). The PASL for health systems is an impactful member of US Medical Affairs (USMA) cross-functional teams, US Medical Affairs Teams (USMAT), and Value Teams (VT).
+ The US PASL drives US HS strategic excellence and optimizes HS and USMA readiness in support of payor access, pharmacoeconomic and scientific exchange aligned to Global V&I plan priorities. This is a regionally based position (US) in our company's Research and Development (R&D) division.
** Responsibilities and Primary Activities*
* + Responsible for the direction, coordination, implementation, control, and execution of USMA and HS payor and access strategy while remaining aligned to global medical and commercial strategy, commitments, and goals. Leads the US HS integrated Field Medical (FM) plan process in collaboration with US HS Executive Director (US HS ED), US HS Senior PASL, US HS Team Leads, and other members of the global and regional cross-functional teams.
+ Possesses relevant medical affairs experience to guide and direct payor and access strategy in alignment with organizational priorities and unmet needs
+ Collects, analyzes, and communicates scientific insights from US HS Medical Affairs Director (MAD) field engagements to inform company strategies across our research division/Value & Implementation, which includes Global Medical & Scientific Affairs (GMSA) and Outcomes Research (OR), and Commercial.
+ Serves as US Health Systems interface between GMSA, Commercial, and other relevant headquarters (HQ) functions and the US HSTeam
+ Identifies and prioritizes US HS field resources, training needs, and activities across the portfolio to optimize HS MAD Field Team readiness
+ Collaborates with key stakeholders to define/implement strategic congress priorities for US HS and coordinates planning of HS MAD activities at key scientific congresses
+ Continuously scans the healthcare environment and quality landscape to analyze emerging trends in the therapeutic and competitive landscape, in addition to market access to optimize US Field HS Team capabilities
+ Represents USMA HS, in partnership with GMSA, in Expert Input Forums or Advisory Boards, as needed
** Required Qualifications, Skills, & Experience*
* ** Minimum*
* + Advanced healthcare/science degree (MD, PhD, or PharmD)
+ 5+ years of prior pharmaceutical industry experience, (preferably Field Medical experience or equivalent biotech/pharmaceutical/Medical Affairs strategy experience), OR 5+ years of experience working in quality/managed care, with demonstrated scientific acumen OR equivalent
+ Demonstrated ability to create and implement a strategic plan
+ Excellent interpersonal, communication, networking, and results-oriented project management skills
+ Thorough knowledge of clinical medicine, US healthcare delivery system structure and function, pharmaco-economics, population health management, quality management, value-based payment, and healthcare delivery policy and trends
+ Demonstrated ability to effectively work in a complex, matrixed environment (promoting inclusion, maintaining trust, and respecting others)
+ Ability to network and partner with important internal and external stakeholders, including cross functional teams, scientific leaders, and key decision makers
+ Knowledge of national and society treatment guidelines, clinical research processes, FDA regulations, and Office of the Inspector General (OIG), Health Insurance Portability and Accountability Act (HIPAA), and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its external stakeholder environment
** Preferred*
* + Prior experience leading complex projects with demonstrated ability to handle multiple projects and priorities simultaneously and function in a fast-paced environment
+ Formal training in pharmaco-economics/outcomes research
eligibleforERP
*
* Required Skills:
*
* Clinical Research, External Collaboration, Managed Care, Medical Affairs, Pharmaceutical Medical Affairs, Pharmacoeconomics, Research and Development, Scientific Communications, Strategic Thinking
** Preferred
Skills:
*
* Current Employees apply HERE ($6687.htmld)
Current Contingent Workers apply HERE ($4020.htmld)
** US and Puerto Rico Residents Only:*
* Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please () if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other…
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