Manager, Research Study Activation

Job not on LinkedIn

🕒 May 28

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

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McKesson

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1833

⚕️ Healthcare Insurance

💊 Pharmaceuticals

🧬 Biotechnology

Healthcare Insurance • Pharmaceuticals • Biotechnology

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

• Responsible for overall study activation activities, including direct supervision and development of staff. • Ensure adherence to standard operating procedures and reporting of data to internal and external groups. • Provide leadership in the study start-up, to include trials in lead, opportunity, and selection. • Oversee the study activation team and liaise with site, sponsor and CRO contacts. • Support the overall site evaluation process from review of opportunity to executive leadership recommendation. • Interface with Sarah Cannon lines of business to develop/foster relationships and understanding of business line needs. • Facilitate business development and relationship management activities with pending and active sites and pharma/CRO partners. • Utilize metrics to drive improvement strategies trial activations for sites and site, sponsor, and CRO partner relationships. • Appropriately escalate unresolved issues to Senior Manager or appropriate level of management. • Drive new initiatives and special projects as directed by Senior Manager, Site Relationships and Support Services.

🎯 Requirements

• The ability to read, understand, and comply with research protocols. • Knowledge of FDA guidelines and GCP. • Resourceful with heightened analytical abilities and problem-solving skills in a fast-paced environment. • Excellent interpersonal skills, detail-oriented and meticulous. • Clinical and/or scientific experience in a research setting required. • Research certification (ACRP or CCRP) preferred.

🏖️ Benefits

• Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being.