Director, GPO Clinical Support, Multispecialty

**Director, GPO Clinical Support, Multispecialty** -------------------------------------------------- Remote \- Texas Job ID JR0145338 Category Pharmacist, Pharmacy Post Date Apr. 08, 2026 McKesson is an impact\-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well\-being of you and those we serve – we care. What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you. The **Director, GPO Clinical Support, Multispecialty** supports the **Vice President, GPO Manufacturer Business Development, MSPL**, by providing clinical and regulatory expertise across McKesson GPO pharmaceutical relationships. This role delivers evidence\-based clinical insight across multiple therapeutic areas, including **Retina, Immunology, Gastroenterology, Rheumatology, Neurology, Endocrinology, and Specialty Injectables**. As a strategic partner to **Business Development, Analytics, Contracting, and Provider Engagement**, the Director, GPO Clinical Support helps shape contracting strategy, strengthen manufacturer engagement, and enhance member value by translating clinical evidence, market dynamics, and regulatory considerations into actionable insights. **Key Responsibilities** * Provide **clinical and regulatory support** for multispecialty GPO pharmaceutical portfolios, including monitoring FDA approvals, label changes, PDUFA timelines, and emerging clinical data. * Conduct **clinical reviews of branded, generic, and biosimilar products** to support contracting, formulary, and value‑based decision‑making. * Summarize and interpret **clinical trial data and regulatory information** for internal cross‑functional partners. * Respond to clinical inquiries related to drug utilization, indications, and regulatory status across multispecialty therapeutic areas. * Partner with **GPO Contracting and Business Development** teams to support manufacturer strategy and engagement discussions. * Support clinical evaluation of **pipeline and pre‑launch assets** under manager guidance. * Contribute to formulary positioning and value narratives through **comparative clinical assessments**. * Participate in manufacturer meetings by providing **clinical background, analysis, and insights**. * Collaborate with **Analytics** teams to contextualize utilization trends, therapeutic class dynamics, and market changes. * Coordinate with **Legal and Compliance** partners on clinical review of contract language and related materials. * Develop and maintain **therapeutic area reference tools**, including drug comparisons by indication, formulation, and route