
Scientific Director – Medical Payer Strategy, Oncology
Posted 5 hours ago

Posted 5 hours ago
This is a fully remote position, open to applicants in Illinois.
• Provide medical and scientific insights into oncology market access, payer strategies, group purchasing organizations, health systems, guidelines, and pathways.
• Create and implement strategies and educational initiatives for payer and healthcare access decision-makers.
• Convert insights from payers and healthcare decision-makers into brand strategies and integrated value evidence plans.
• Lead the medical affairs strategy targeting payers and healthcare decision-makers for assigned therapeutic areas and assets.
• Transform clinical, economic, humanistic, and real-world evidence into distinct value narratives.
• Engage in cross-functional teams including brand, medical affairs, HEOR, and market access.
• Oversee the development and approval of materials for medical affairs access and healthcare decision-maker across various channels.
• Conduct training sessions for Medical Outcomes Science Liaison teams.
• Collaborate on integrated evidence plans with Medical Affairs and HEOR.
• Formulate strategies for collaborative research, thought-leadership forums, and partnerships with payers and healthcare decision-makers.
• Keep abreast of scientific, health economic, access, and healthcare policy trends.
• Contribute to portfolio, therapeutic area, and brand strategies.
• Act as the scientific liaison for regulatory, OEC, and Legal discussions.
• Support medical affairs-sponsored or supported real-world evidence research activities.
• Lead cross-functional teams and functional subteams responsible for therapeutic-area projects.
• Ensure adherence to corporate, divisional, legal, and regulatory policies and requirements.
• Advanced degree: PhD, PharmD, PA, or NP is highly preferred.
• Completion of a residency or additional post-doctoral training is highly preferred.
• Generally, 8 years of experience in the pharmaceutical industry or equivalent is required.
• A solid understanding of managed care is essential.
• Pharmacoeconomic experience is preferred.
• Experience in management and leadership at the project level is necessary.
• Familiarity with strategic initiatives and issues is expected.
• Proven leadership capabilities in a cross-functional setting.
• Ability to engage with both external and internal stakeholders to support global business strategies.
• Capacity to independently advance RWE studies or medical affairs-directed research with minimal supervision.
• Understanding of statistical methodologies is required.
• Knowledge of regulatory guidelines governing RWE is essential.
• Experience in developing strategies and designing RWE protocols is required.
• Exceptional oral and written communication skills are necessary.
• Capability to work primarily independently with limited guidance.
• Must understand and adhere to legal, regulatory, corporate, and divisional standards.
• Paid time off (including vacation, holidays, and sick leave).
• Medical, dental, and vision insurance.
• 401(k) plan.
• Eligibility to partake in long-term incentive programs.
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