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

Posted 5 hours ago
This is a fully remote position, open to applicants in California.
• Contribute medical and scientific expertise to oncology market access, including payer, group purchasing organization, health system, guideline, and pathway strategies.
• Design and implement strategies and educational initiatives targeted at payer and healthcare access decision-makers.
• Convert insights from payers and healthcare decision-makers into brand strategies and comprehensive value evidence plans.
• Direct medical affairs strategies for payers and healthcare decision-makers related to specific therapeutic areas and assets.
• Transform clinical, economic, humanistic, and real-world evidence into unique value propositions.
• Engage with cross-functional teams in brand management, medical affairs, and market access.
• Offer medical, scientific, pharmacoeconomic, and healthcare landscape insights for portfolio and product strategies.
• Oversee the creation and approval of medical affairs access and healthcare decision-maker field materials across various channels.
• Conduct training sessions for Medical Outcomes Science Liaison teams.
• Collaborate with Medical Affairs and HEOR to develop integrated evidence plans.
• Formulate strategies for collaborative research with payers/healthcare decision-makers, thought-leadership initiatives, and external partnerships.
• Keep abreast of trends in scientific research, health economics, access, and healthcare policy.
• Provide strategic insights for portfolio, therapeutic area, and brand development.
• Act as the scientific liaison for discussions involving regulatory, OEC, and Legal teams.
• Support medical affairs-sponsored or endorsed real-world evidence research endeavors.
• Lead cross-functional and sub-teams in specific therapeutic area projects.
• Ensure adherence to corporate, divisional, legal, and regulatory standards.
• Advanced degree; PhD, PharmD, PA, or NP is strongly preferred.
• Completion of a residency or additional post-doctorate training is highly favored.
• Generally, 8 years of experience in the pharmaceutical industry or a related field is required.
• A solid understanding of managed care is essential.
• Experience in pharmacoeconomics is preferred.
• Proven management and leadership skills at the project level.
• Experience with strategic initiatives and challenges.
• Demonstrated leadership abilities in a cross-functional setting.
• Capability to engage with both external and internal stakeholders to bolster global business strategies.
• Ability to independently advance RWE studies or medical affairs-directed research with minimal supervision.
• Familiarity with statistical methodologies.
• Understanding of regulatory requirements related to RWE.
• Experience in strategizing and designing RWE protocols.
• Exceptional oral and written communication skills.
• Ability to work primarily independently with limited oversight.
• Must adhere to all relevant legal, regulatory, corporate, and divisional standards.
• Paid time off that includes vacation, holidays, and sick leave.
• Comprehensive medical, dental, and vision insurance.
• 401(k) retirement plan.
• Eligibility to engage in long-term incentive programs.
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