Clinical Research Protocol Educator - Remote

Position: Clinical Research Protocol Educator - Remote US

It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community‑based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission‑driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world.

Job Description As the Clinical Research Protocol Educator you will direct the design, plan, delivery and evaluation of clinical trial related training activities of Sarah Cannon colleagues. Your training primarily includes Research Nurses but may also include Research Coordinators, non‑clinical research staff, and Clinical Site personnel.

This is a remote position based in the US; relocation assistance and visa sponsorship are not available.

Duties include and are not limited to:

• You will attend and participate in Investigator and Site start up meetings with the responsibility to disseminate appropriate information to the Clinical Operations staff
• You will develop and participate in the delivery of training for new protocols and determine the delivery mechanism, timing and frequency
• You will develop and utilize learning aids such as self‑study guides, demonstration models, multimedia visual aids, computer tutorials and reference materials to educate and train applicable staff
• You will develop presentations and facilitate groups, workshops and programs to enhance strategic site clinic and Sarah Cannon research staff knowledge
• You will complete regimen templates for HER systems for current and upcoming protocols

Other duties as assigned.

Qualifications for success include:

• An Associate Degree;
  Bachelor Degree preferred
• Extensive oncology knowledge base of all 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 the conduct of clinical trials involving human subjects for Investigator and Sponsor requirements
• Knowledge and understanding of the principles, processes, and ethical considerations in clinical trials involving 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
• Research Certification (ACRP or CCRP) preferred
• Oncology Certification (OCN) preferred

About Sarah Cannon Research Institute Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community‑based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country.

It has conducted more than 850 first‑in‑human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into…