Research Nurse Educator, Sarah Cannon Research Institute

Directs the design, plan, delivery and evaluation of clinical trial related training activities of Sarah Cannon Research Institute (SCRI) employees. This primarily includes Research Nurses but is not limited, and also include Research Coordinators, non-clinical research staff, and Clinical Site personnel.

Duties include but are not limited to: Attend and participate in Investigator and Site start up meetings with the responsibility to disseminate appropriate information to the Clinical Operations staff Develop and participate in the delivery of training for new protocols, including:

Create training materials

Determine delivery mechanism, timing and frequency

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

Develop presentations and facilitate groups, workshops and programs to enhance strategic site clinic and SCRI research staff knowledge

Complete regimen templates for EHR systems for current and upcoming protocols.

Participate in Protocol Review Committee that includes attending meetings and evaluation and assessing protocols in advance to determine complexity, identify risks associated with a trial and operational and implementation challenges

Contribute timely and completely to centralized training files for each employee as appropriate by forwarding all necessary information to the Human Resources Director

Serve as clinical resource for development, implementation and maintenance of electronic systems as needed Serve as clinical resource for triage and addressing incoming AskSarah calls that are related to clinical matter

Create and update the Program Development Study Lead Transmittal (PDSLT) worksheet with specific study details for the sites to use as a tool at the time of study initiation. Review Informed

Consent templates and submit editing recommendations to the Regulatory Affairs Specialists. All other duties as assigned. #LI-NL1 IND01

Must have extensive oncology knowledge base of all major cancer types including disease-related symptom management, standard treatment options, and treatment-related side effect management

Must have knowledge of federal and state regulations and ICH guidelines pertaining to the conduct of clinical trials involving human subjects for Investigator and Sponsor requirements.

Must have knowledge and understanding of the principles, processes, and ethical considerations in clinical trials involving human subjects.

Must have a general working knowledge of the guidelines, standards and operating requirements of Institutional Review Boards

Foster effective working relationships within a team environment

Work at a fast pace while maintaining attention to detail Communicate and work effectively with a diverse team of professionals

Associate's degree required, Bachelor's degree preferred

1-3 years' oncology research experience required

RN/BSN preferred, ACRP, CCRP, OCN preferred