What are the responsibilities and job description for the COORD STUDY ACTIVATION SR position at Moffitt Cancer Center Careers?
At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America’s Best Large Employers and America’s Best Employers for Women, Computerworld magazine’s list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time’s Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet® designation in recognition of its nursing excellence.
Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999.
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision.
Summary
Job Summary:
The Coordinator Study Activation Senior (CSA Sr) is responsible for initiating the startup of a high volume of complex clinical research protocols and seeing them through to activation, in accordance with institutional and industry standards at Moffitt Cancer Center. The role works independently to facilitate and complete operational tasks associated with the startup of a large volume of clinical research protocols. This includes managing them through to activation at the cancer center in accordance with institutional and industry standards.
This position develops study related documents, anticipates potential obstacles to activation and proactively addresses them to avoid delay of clinical trial activation.
The incumbent is required to serve as a subject-matter expert and has a high proficiency regarding the knowledge of protocol requirements and good clinical practices as set forth by Federal regulations.
Minimum Experience Required:
Bachelor's degree with four (4) years of experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination) of which three (3) years in clinical trial activation is required.
**In lieu of a Bachelors degree:
- Associates degree with six (6) years of experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination) of which three (3) years in clinical trial activation is required OR
- High school diploma with eight (8) years of experience in clinical trials (as noted above) of which three (3) years required in clinical activation may be considered.
