Director, Medical Payer Strategy – Eye Care, Neurotoxins

atAbbVieRemoteUS flagCaliforniaFull-timeMedical DirectorLead$182k – $346k/year

Posted Aug 25

This is a fully remote position, open to applicants in California.

πŸ“‹ Description

β€’ Spearhead the development and implementation of market access strategies, including payer, IDN, guidelines, and clinical pathway scientific strategies aimed at access decision-makers.

β€’ Formulate and execute Medical Affairs access/HCDM strategies and tactics across payer, distribution, IDN, and GPO channels.

β€’ Offer scientific and pharmacoeconomic expertise in market access to cross-functional teams.

β€’ Engage in the development of global gap assessments and contribute medical market access insights to Integrated Evidence Plans through IEST.

β€’ Create strategic resources and deliver scientific and technical training.

β€’ Lead the creation of HCDM-focused medical pharmacoeconomic materials, medical education programs, advisories, and symposia.

β€’ Support the scientific review, development, execution, and communication of medical affairs-sponsored or supported RWE research initiatives.

β€’ Identify and implement strategic initiatives in collaboration with HCDM-focused professional organizations.

β€’ Develop and oversee the approval process for field materials for the Value & Access MOSL team.

β€’ Direct the RWE plan in conjunction with HEOR, manage the generation of pertinent data, and train key stakeholders.

β€’ Formulate strategies for potential collaborative customer research focused on access/HCDM.

β€’ Track scientific, health economic, and payer policy advancements through conferences and medical literature.

β€’ Represent AbbVie at industry conferences and events, advocating for patient access and presenting on payer strategies.

β€’ Act as the scientific team liaison for regulatory, OEC, and Legal discussions.

β€’ Assist in the development of Medical Affairs resources and provide training for Value & Access Field teams.

β€’ Ensure adherence to corporate, divisional, legal, regulatory, and healthcare standards.


⛳️ Requirements

β€’ Advanced degree: PhD, PharmD, PA, or NP is strongly preferred.

β€’ Generally, a minimum of 8 years of experience in the pharmaceutical industry or a similar field.

β€’ A significant understanding of managed care is essential.

β€’ Experience in pharmacoeconomics is preferred.

β€’ Proven management and leadership experience at the project level.

β€’ Background in handling strategic initiatives and relevant issues.

β€’ Demonstrated leadership capabilities in a cross-functional setting.

β€’ International experience is advantageous.

β€’ Experience in Eye Care or Neuroscience is preferred.

β€’ Capability to engage with external and internal stakeholders to support global business strategies.

β€’ Ability to independently advance RWE studies or medical affairs-directed research with minimal supervision.

β€’ Familiarity with statistical methodologies.

β€’ Understanding of regulatory requirements governing RWE.

β€’ Experience in the development and design of RWE protocols.

β€’ Exceptional oral and written communication skills.

β€’ Ability to work primarily independently with limited guidance.

β€’ Must adhere to relevant corporate and divisional policies, as well as legal and regulatory obligations.


🏝️ Benefits

β€’ Paid time off (including vacation, holidays, and sick leave).

β€’ Medical, dental, and vision insurance coverage.

β€’ 401(k) retirement plan.

β€’ Eligibility to participate in long-term incentive programs.

β€’ Commitment to equal opportunity employment.

β€’ Provision of reasonable accommodations for applicants in the US and Puerto Rico.

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