[Hiring] Clinical Research Protocol Educator @Sarah Cannon Research Institute

Role 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.

• 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

• 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.

Benefits

• Comprehensive benefits to support physical, mental, and financial well-being.
• Competitive compensation package determined by performance, experience, skills, equity, regular job market evaluations, and geographical markets.
• Other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

Company Description

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 clinical trials at more than 200 locations in 20+ states across the U.S.