Study Lead Coordinator

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🔥 0 minutes ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Manage SCRI’s Clinical Trial lead management inbox • Send initial responses to pharma, biotech, and CRO contacts • Collect required documents for scientific-interest review • Create and maintain the Lead Management tracking system • Track lead-management metrics and research sites in appropriate systems • Upload study documents and create folders in CTMS and Florence eBinder • Process, facilitate, and track nondisclosure agreements • Create and update legacy CTMS systems and Florence • Support the feasibility process and site provisioning • Follow detailed Lead Management procedures • Escalate lead-management issues to the supervisor • Work closely with the Study Lead Manager to set goals and align objectives • Complete other special projects as needed • Serve as a point of contact for internal Sarah Cannon departments, physician leaders, strategic-site staff, CROs, and pharmaceutical companies for study intake and lead tracking

🎯 Requirements

• Typically, college graduate or equivalent experience • Knowledge of pharmaceutical industry, regulatory process, clinical trials, and medical terminology • At least 1 year of experience within clinical research, preferably within trial management • Professional writing and communication skills • Organized and prioritizing capabilities • Computer skills, including Word, Excel, Microsoft Outlook, and Smartsheet • Problem-solving skills in a fast-paced environment • Interpersonal skills and attention to detail • Ability to follow specific, outlined, and detailed procedures • Entry-level professional position with on-the-job training

🏖️ Benefits

• Comprehensive Total Rewards package supporting physical, mental, and financial well-being • Competitive compensation package • Annual bonus or long-term incentive opportunities may be offered • Resources and opportunities to grow and develop a fulfilling career • Inclusive environment with strong values • Balanced life