Clinical Research Protocol Educator

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🔥 3 minutes ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟢 Junior

🧪 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

• Direct the design, planning, delivery, and evaluation of clinical trial-related training activities for Sarah Cannon colleagues • Train Research Nurses, Research Coordinators, non-clinical research staff, and Clinical Site personnel • Attend and participate in Investigator and Site start-up meetings • Disseminate appropriate information to Clinical Operations staff • Develop and participate in delivering training for new protocols • Determine training delivery mechanisms, timing, and frequency • Develop and use learning aids, including self-study guides, demonstration models, multimedia visual aids, computer tutorials, and reference materials • Develop presentations and facilitate groups, workshops, and programs • Complete regimen templates for HER systems for current and upcoming protocols • Perform other duties as assigned

🎯 Requirements

• Associate Degree required • Bachelor Degree preferred • Extensive oncology knowledge covering major cancer types, disease-related symptom management, standard treatment options, and treatment-related side effect management • Knowledge of federal and state regulations and ICH guidelines for clinical trials involving human subjects • Knowledge of clinical trial principles, processes, and ethical considerations • Knowledge of Institutional Review Board guidelines, standards, and operating requirements • At least one year of oncology experience • At least one year of research experience • Research Certification (ACRP or CCRP) preferred • Oncology Certification (OCN) preferred • Must be based in the US • Relocation assistance and visa sponsorship are not available

🏖️ Benefits

• Comprehensive benefits supporting physical, mental, and financial well-being • Competitive compensation package • Annual bonus or long-term incentive opportunities may be offered • Remote work arrangement

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