COORD STUDY ACTIVATION II

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 II (CSA II) is responsible for initiating the startup of clinical research protocols and seeing them through to activation, in accordance with institutional and industry standards at Moffitt Cancer Center. The incumbent is expected to work independently with minimal guidance and direction from the supervisor, manager, and Principal Investigator to develop study-related documents, anticipate potential obstacles to activation and pro-actively address them to avoid delay of clinical trial activation.

The role will perform diverse complex administrative duties requiring analysis, sound judgment, and a of knowledge of study conduct. This position has a strong understanding of project management and possesses strong problem-solving and communication skills.

The incumbent is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by Federal regulations.

Job Requirements

Bachelor's degree with three (3) years' experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination) of which two (2) years' experience in clinical trial activation is required.

• In lieu of Bachelor's degree:
• an associate's degree and five (5) years' experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination of which two 2) years' experience in clinical trial activation is required, OR
• a high school diploma and seven (7) years' experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination in which two (2) years of experience in clinical trial activation is required.