Scientific Director – Medical Payer Strategy, Oncology

atAbbVieRemoteUS flagNew JerseyFull-timeMedical DirectorLead$160.5k – $305k/year

Posted 1 day ago

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

πŸ“‹ Description

β€’ Offer medical and scientific expertise in oncology market access, including strategies for payers, group purchasing organizations, health systems, guidelines, and pathways.

β€’ Create and implement medical market access initiatives, which encompass strategies for payer and healthcare access decision-makers along with educational programs.

β€’ Convert insights from payers and healthcare decision-makers into strategic recommendations.

β€’ Collaborate across functions with teams in commercial, HEOR, and medical affairs within a highly matrixed setting.

β€’ Spearhead the development of medical affairs strategies for payers and healthcare decision-makers concerning specific therapeutic areas and assets.

β€’ Transform clinical, economic, humanistic, and real-world evidence into unique value narratives.

β€’ Define access strategies, prioritize brands and portfolios, and inform enterprise decisions.

β€’ Oversee the creation and approval of field and omnichannel medical affairs access materials.

β€’ Conduct training sessions for Medical Outcomes Science Liaison teams.

β€’ Collaborate on integrated evidence plans with Medical Affairs and HEOR.

β€’ Formulate strategies for collaborative research with payers and healthcare decision-makers, thought-leadership forums, and external partnerships.

β€’ Track trends in scientific, health economics, access, and healthcare policy through conferences, insight gathering, and stakeholder engagement.

β€’ Contribute to portfolio, therapeutic area, and brand strategies.

β€’ Act as the scientific liaison for essential regulatory, OEC, and legal discussions.

β€’ Support medical affairs-sponsored or supported real-world evidence research activities.

β€’ Lead cross-functional and functional subteams responsible for specific therapeutic area projects.

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


⛳️ Requirements

β€’ Advanced degree (PhD, PharmD, PA, or NP is highly preferred).

β€’ Residency or additional postdoctoral training is highly preferred.

β€’ Generally, 8 years of experience in the pharmaceutical industry or equivalent.

β€’ Strong understanding of managed care is required.

β€’ Pharmacoeconomic experience is preferred.

β€’ Experience in management and leadership at the project level.

β€’ Familiarity with strategic initiatives and issues.

β€’ Demonstrated leadership abilities in a cross-functional context.

β€’ Capacity to engage externally and internally to support global business strategy.

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

β€’ Proficient knowledge of statistical methodologies.

β€’ Awareness of regulatory requirements surrounding RWE.

β€’ Experience in strategy development and RWE protocol design.

β€’ Exceptional oral and written communication skills.

β€’ Comprehension of legal and regulatory requirements along with the healthcare landscape.

β€’ Must adhere to applicable corporate and divisional policies and procedures.


🏝️ Benefits

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

β€’ Medical, dental, and vision insurance.

β€’ 401(k) plan.

β€’ Long-term incentive programs.

β€’ Flexible hybrid work arrangement.

β€’ Equal opportunity employer, including support for Veterans and individuals with disabilities.

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