Clinical Scientist

Job not on LinkedIn

🔥 0 minutes ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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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

• Provide scientific assistance and support for Sarah Cannon Medical Directors and study teams overseeing SCRI trials • Provide clinical, therapeutic, and scientific expertise to study teams • Support creation of trial deliverables • Conduct ongoing medical data review focused on patient safety and efficacy • Follow standard operating procedures, ICH-GCP, and applicable regulatory requirements • Serve as scientific point of contact for industry-sponsored and investigator-initiated trials • Collaborate with medical writing during clinical study protocol development and attend protocol development meetings • Review clinical study protocols, informed consent forms, investigator brochures, case report forms, clinical study reports, TFL shells, TFLs, study documentation, and publications • Perform medical data review and assessments of safety and efficacy data • Review clinical research data including patient demographics, medical and disease history, concomitant medications, laboratory values, adverse events, disease response verification, and overall data quality • Perform other duties as assigned

🎯 Requirements

• Bachelor’s Degree (4-year program) required • Minimum 2+ years of experience analyzing data and science in clinical research and/or laboratory-based research or within the pharmaceutical or CRO environment • Prior work experience in a highly-detailed role such as nursing or scientific research • Prior work experience in a collaborative environment taking initiatives when needed such as process improvement • Experience in oncology clinical research and/or oncology-focused laboratory-based research preferred • Familiarity with medical data review preferred • Must be based in the US

🏖️ Benefits

• Total Rewards package including comprehensive benefits supporting physical, mental, and financial well-being • Competitive compensation package • Annual bonus or long-term incentive opportunities may be offered • Relocation assistance is not available • Visa sponsorship is not available