Clinical Program Scientist I

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🕒 4 days ago

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McKesson

10,000+ employees

Founded 1833

💼 Consulting

📦 Logistics

🏥 Healthcare

Consulting • Logistics • Healthcare

McKesson is a diversified healthcare leader specializing in pharmaceutical distribution, medical supplies, and healthcare services. Their solutions facilitate patients' access to life-changing therapies, support efficient operations for pharmacies, health systems, and clinics, and address critical issues such as drug shortages through a resilient supply chain. McKesson provides comprehensive services such as pharmacy management software, consulting, and technology solutions for specialty practices, focusing on improving health outcomes and advancing the pharmaceutical industry. They work closely with biopharma companies to enhance medication access, adherence, and commercialization while supporting oncology and biopharma practices through data-driven insights and real-world evidence.

📋 Description

• Deliver scientific, administrative, and operational support to the Associate Director and/or Director in managing one or more SCRI Research Programs • Focus on advancing program objectives through disease-focused expertise and collaborative project execution • Build and maintain working relationships across the organization relevant to the role • Lead disease program related meetings with oversight from Associate Director, as appropriate • Attend and support Physician Program Director 1:1 meetings • Utilize tools to track and identify study gaps • Collaborate with clinical program associate on one-page study summary updates; review document for accuracy • Provide new study evaluation and start-up support • Support executive committee meetings by sending agenda & meeting summary emails • Prepare all other applicable content to support meetings • Maintain records and documents decisions from Leads Meetings

🎯 Requirements

• PhD strongly preferred • 5+ years working in a scientific capacity within clinical research • Oncology experience and clinical research (phase I – IV) experience required • Ability to pull scientific literature to support research projects • Willingness to develop disease-specific and drug development expertise required to support a SCRI Research Program • Ability to work in cross-functional, multi-cultural teams • Excellent time management skills • Strong organizational skills and ability to re-prioritize tasks as necessary • Strong verbal and written communication skills • Strong ability to function in a dynamic environment and adapt to changing needs of program • Highly resourceful

🏖️ Benefits

• Comprehensive benefits to support physical, mental, and financial well-being• Competitive compensation package determined by several factors including performance, experience, skills, and geographical markets

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