Spvr Clinical Trials Activation

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, Diversity Inc 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.

With oversight from the Manager, Clinical Trial Activation, and in collaboration with the faculty and investigators, the Supervisor provides basic day-to-day supervision and oversight of the assigned clinical research operations program staff to ensure implementation of good clinical practices as set forth by Federal regulations. The Supervisor has direct reporting responsibilities and supports the recruiting, training, development, and performance management of staff.

Operationally, the Supervisor focuses on the day-to-day conduct of study activation and quality assurance needs, providing problem solving and troubleshooting expertise. The Supervisor may be expected to identify process improvement opportunities, collaborate with the team to develop creative solutions, lead implementation, and track success through defined metrics.

In addition to supervisory responsibilities, the Supervisor, Clinical Trial Activation, will maintain a percent (%) of effort, as determined by the Manager, Clinical Trial Activation, dedicated to Coordinator Study Activation responsibilities.

• Bachelor's Degree Healthcare, life science or relevant degree.
• Bachelor's degree with six (6) years of experience in clinical trials (e.g., patient facing coordination, data management, regulatory or other clinical research coordination) inclusive of two (2) years in clinical trial activation.
• SOCRA, CCRP or equivalent