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

The Manager Clinical Trials Regulatory Compliance is responsible for long- and short-term planning and oversight of regulatory activities. Interprets federal and state regulations, corporate policy, and clinical research best practices to develop and implement strategies for the earliest possible approval of regulatory submission. Advises and manages the regulatory teams, and reviews ongoing projects. Plans, schedules and directs activities and programs through regulatory staff. Negotiates with outside agencies (IRBs) as needed to resolve key regulatory issues and expedite approvals of clinical trials at Moffitt Cancer Center. Communicates regulatory submission status to programs and investigators regularly.

Education and Experience Required:

Qualified candidates will have a minimum of a Bachelor's Degree, a Master's Degree is preferred. This position requires 5 years relevant clinical research regulatory experience. Previous supervisory or management experience strongly preferred, knowledgeable in CCSG requirements, as well as quality systems/auditing experience.

Preferred:

Certified IRB Professional (CIP)