Clinical Research Protocol Educator - Remote US

Sarah Cannon Research Institute • Nashville, TN

2d • Remote

About The Position

The Clinical Research Protocol Educator directs the design, planning, delivery, and evaluation of clinical-trial-related training for Sarah Cannon Research Institute colleagues. Training primarily serves Research Nurses and may also include Research Coordinators, non-clinical research staff, and Clinical Site personnel. This is a remote position based in the United States; relocation assistance and visa sponsorship are not available.

The role participates in Investigator and Site start-up meetings and disseminates appropriate information to Clinical Operations staff. It develops and delivers protocol training, determines how and when training is provided and how often it occurs, creates learning aids, and facilitates presentations, groups, workshops, and programs to build knowledge among site clinic and Sarah Cannon research staff. The educator also completes regimen templates for HER systems for current and upcoming protocols and performs other duties as assigned.

Requirements

• Associate degree.
• Extensive oncology knowledge of major cancer types, including disease-related symptom management, standard treatment options, and treatment-related side-effect management.
• Knowledge of federal and state regulations and ICH guidelines pertaining to clinical trials involving human subjects, including Investigator and Sponsor requirements.
• Knowledge and understanding of the principles, processes, and ethical considerations involved in clinical trials with human subjects.
• Knowledge of the guidelines, standards, and operating requirements of Institutional Review Boards.
• At least one year of oncology experience.
• At least one year of research experience.

Nice To Haves

• Bachelor's degree.
• Research certification (ACRP or CCRP).
• Oncology certification (OCN).

Responsibilities

• Attend and participate in Investigator and Site start-up meetings, disseminating appropriate information to Clinical Operations staff.
• Develop and participate in delivering training for new protocols, determining the delivery mechanism, timing, and frequency.
• Develop and use learning aids such as self-study guides, demonstration models, multimedia visual aids, computer tutorials, and reference materials.
• Develop presentations and facilitate groups, workshops, and programs to enhance the knowledge of strategic site clinic and Sarah Cannon research staff.
• Complete regimen templates for HER systems for current and upcoming protocols.
• Perform other duties as assigned.

Benefits

• Comprehensive Total Rewards benefits supporting physical, mental, and financial well-being.
• Competitive compensation package.
• An annual bonus or long-term incentive opportunities may be offered.

What This Job Offers

• Job Type: Full-time
• Education Level: Associate degree