Senior Clinical Team Lead

Job not on LinkedIn

🔥 16 hours ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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• Open for 1 day.
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• No salary listed.

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McKesson

WebsiteLinkedInAll Job Openings

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

• Work closely with Clinical Project Managers to facilitate collaboration between project teams, research sites, and clinical trial sponsors • Ensure clinical tasks meet client and Sarah Cannon expectations and comply with contracts, protocols, project plans, ICH-GCP guidelines, and SOPs • Provide leadership in developing clinical trials and related documents • Assist in planning and tracking assigned clinical activity across start-up, interim, and close-out phases • Assist in defining and managing project resource needs and contingency plans • Assist in planning trial budgets, communicating deviations, and proposing solutions • Identify and present project issues and facilitate cross-functional resolutions • Assist with creation and maintenance of clinical project documents and plans • Develop and conduct study team training • Set up clinical trial monitoring systems and study tools • Perform other duties as assigned

🎯 Requirements

• Bachelor Degree highly preferred; appropriate experience may be substituted for education • 3+ years' work experience as a Sr CRA, CTL or equivalent role • 3+ years direct oncology experience, Phase I - III • Experience managing study timelines, deliverables, and/or vendors • Prior experience mentoring and/or training less senior team members • Demonstrated leadership skills • Must be based in the US

🏖️ Benefits

• Comprehensive benefits supporting physical, mental, and financial well-being • Annual bonus or long-term incentive opportunities may be offered • Relocation assistance is not available • Visa sponsorship is not available

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