What are the responsibilities and job description for the SPVR REGULATORY AFFAIRS CTO 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:
With oversight from the responsible CTO Manager, and in collaboration with the faculty and investigators, the Supervisor provides basic day-to-day supervision of the clinical research regulatory staff and operations for the research programs assigned with the goal to support program regulatory needs. The Supervisor supports the recruiting, training, development, and performance management of assigned staff. Operationally, the Supervisor focuses on the day to day study start up, trial regulatory, and quality assurance needs, providing problem solving and troubleshooting expertise. The Supervisor will be expected to identify process improvement opportunities, collaborate with their team to develop creative solutions, lead/delegate implementation, and track success through defined metrics.
Requirements:
- Bachelors Degree
- Six (6) years previous clinical research regulatory experience.
- Certification: SoCRA or ACRP, or equivalent, must be maintained per national group requirements.
- High level competency in Microsoft Office Suite - Excel and Word required
- Demonstrated leadership and team building skills.
- Demonstrated diplomacy, tact, and professional demeanor.
- Strong collaborative, prioritization and organizational skills.
Preferred:
- Masters Degree
- Oncology trials knowledge and experience
- Supervisory, or Team Lead experience
- OnCore® CTMS experience
