Scientific Director – Medical Payer Strategy, Oncology

🔥 9 minutes ago

🌽 Illinois – Remote

🌽 Illinois – Remote

💵 $160.5k - $305k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.

📋 Description

• Provide medical and scientific input into oncology medical market access, payer, group purchasing organization, health system, guideline, and pathway strategies • Develop and execute payer and healthcare access decision-maker strategies and educational initiatives • Translate payer and healthcare decision-maker insights into brand strategies and integrated value evidence plans • Lead medical affairs payer/healthcare decision-maker strategy for assigned therapeutic areas and assets • Translate clinical, economic, humanistic, and real-world evidence into differentiated value narratives • Participate in cross-functional brand, medical affairs, HEOR, and market access teams • Lead development and approval of medical affairs access/healthcare decision-maker field and omnichannel materials • Lead and deliver training to Medical Outcomes Science Liaison teams • Partner on integrated evidence plans with Medical Affairs and HEOR • Develop strategies for payer/healthcare decision-maker collaborative research, thought-leadership forums, and external partnerships • Monitor scientific, health economic, access, and healthcare policy trends • Provide input into portfolio, therapeutic area, and brand strategies • Serve as the scientific team interface for regulatory, OEC, and Legal discussions • Assist with medical affairs-sponsored or supported real-world evidence research activities • Lead cross-functional and functional subteams responsible for therapeutic-area projects • Ensure compliance with applicable corporate and divisional policies and legal and regulatory requirements

🎯 Requirements

• Advanced education: PhD, PharmD, PA, or NP highly preferred • Residency or additional post doctorate 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 • 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 understand and comply with legal, regulatory, corporate, and divisional requirements

🏖️ Benefits

• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Eligibility to participate in long-term incentive programs

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