Job Description: Drive development and execution of market access payer, IDN, guidelines, and clinical pathway scientific strategies across access decision-makers Develop and execute Medical Affairs access/HCDM strategy and tactics across payer, distribution, IDN, and GPO channels Provide market access scientific and pharmacoeconomic subject matter expertise to cross-functional teams Participate in global gaps assessment development and provide medical market access input into Integrated Evidence Plans via IEST Develop strategic resources and provide scientific and technical training Lead HCDM-focused medical pharmacoeconomic materials, medical education programs, advisories, and symposia Assist with scientific review, development, execution, and communication of medical affairs-sponsored or supported RWE research Identify and execute strategic initiatives with HCDM-focused professional organizations Create and manage approval of field materials for the Value & Access MOSL team Lead the RWE plan with HEOR, oversee generation of relevant data, and train key stakeholders Develop strategy for potential access/HCDM collaborative customer research Monitor scientific, health economic, and payer policy developments through conferences and medical literature Represent AbbVie at industry conferences and events, presenting on payer strategy and advocating for patient access Serve as scientific team interface for regulatory, OEC, and Legal discussions Support development of Medical Affairs resources and train Value & Access Field teams Ensure compliance with corporate, divisional, legal, regulatory, and healthcare requirements Requirements: Advanced education: PhD, PharmD, PA, or NP highly preferred Typically 8 years’ experience in the pharmaceutical industry or equivalent Substantial understanding of managed care required Pharmacoeconomic experience preferred Management and leadership experience at project level Experience with strategic initiatives and issues Proven leadership skills in a cross-functional environment International experience is a plus Experience in Eye Care or Neuroscience preferred Ability to interact externally and internally to support global business strategy Ability to advance RWE studies or medical affairs-directed research independently with little supervision Knowledge of statistical methodology Knowledge of regulatory requirements governing RWE Experience in development strategy and design of RWE protocols Excellent oral and written communication skills Ability to work mostly independently with limited guidance Must comply with applicable corporate and divisional policies, legal and regulatory requirements Benefits: Paid time off (vacation, holidays, sick) Medical, dental, and vision insurance 401(k) Eligibility to participate in long-term incentive programs Equal opportunity employer Reasonable accommodations for US and Puerto Rico applicants