Posting Description: The coordinator will be responsible for all IRB submissions, recruitment and enrollment of study participants, maintaining clinical trial records, and acting as a liaison between the funding agency, COMIRB, grants and contracts, the principal investigator and the department administrator. This position will provide both research and administrative support. The research Responsibilities will include: 1. COMIRB paperwork and communication 2. Recruit and enroll study participants 3. Interview human subjects participating in a clinical trial 4. Complete study visits 5. Maintain clinical trial records 6. Record data results 7. Data entry 8. Obtain and process study samples 9. Track patient participation 10. Abstract data from patient charts 11. Tabulate research data 12. Validate quality of data elements/data editing 13. Ensure study protocol is being followed 14. Interact with coordinating center for this multi-center randomized clinical trial 15. Interact with local satellite centers participating in this study Administrative responsibilities may include scheduling research meetings and appointments as well as assisting with other administrative duties as needed. Salary commensurate with skills and experience. The University of Colorado offers a full benefits package. Information on University benefits programs, including eligibility, is located at http://www.cu.edu/pbs/. The University does check references as part of the employment process, and selection committee members may choose to contact work references during the search process other than those listed in your application. The University of Colorado Denver is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees prior to their employment. The University of Colorado is committed to diversity and equality in education and employment.
Minimum Qualifications: This position requires a minimum of a bachelor's degree and an RN degree. Previous work experience in a clinical research setting specifically study coordination of clinical trials necessary. Must have a current Colorado RN license
Required Competencies/Knowledge, Skills, and Abilities:
Desired Qualifications: Experience coordinating multi-site clinical trials. Experience processing research samples or willingness to be trained strongly desired as well as experience with type 1 diabetes.
Campus: Anschutz Medical Campus