Clinical Research Protocol Educator

McKesson

. Direct the design, planning, delivery, and evaluation of clinical trial-related training activities for Sarah Cannon colleagues .

Posted 11/6/2026full-timeRemote • Tennessee • United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive oncology knowledge and experience in clinical trial principles, processes, and ethical considerations. Proficient in developing and delivering training programs and materials for clinical trial-related activities.

Highest-signal resume keywords

Oncology KnowledgeClinical Trial PrinciplesResearch Certification (ACRP or CCRP)Oncology Certification (OCN)Training Development and Delivery

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesRegimen Templates for HER SystemsTraining Delivery MechanismsLearning Aid DevelopmentPresentation Development

Soft Skills

Facilitation SkillsCommunication SkillsGroup Workshop Leadership

Tools & Technologies

Multimedia Visual AidsComputer TutorialsSelf-Study Guides

Certifications & Qualifications

Research Certification (ACRP or CCRP)Oncology Certification (OCN)

Industry Keywords

OncologyClinical TrialsICH GuidelinesInstitutional Review Board GuidelinesFederal and State Regulations

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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