Job Details
Title: Regulatory Startup Project Coordinator
Company: Moffitt Cancer Center
Location: Tampa, FL
Regulatory Startup Project Coordinator (Req#42847)
Essential Job Functions:
- Responsible for shepherding clinical research projects through the study start up process and oversees the development of study related documents
- Work with Clinical Trials Office training staff to provide new and ongoing education to clinical research staff on Study Activation Procedures
- Primary liaison for regulatory protocol activation issues for internal and external customers; meets with team regularly to provide progress update
- Work on quality metrics for the study activation processes
Credentials and Qualifications:
- Bachelor's degree required (Master's degree preferred)
- Five (5) years' experience in clinical research (2 of the 5 years must be in a research study start up or regulatory position)
- CCRP/CCRC or equivalent certification preferred
- Working knowledge of Food and Drug Administration and other regulatory requirements
- Strong scientific knowledge and research skills
- Oncology experience preferred (2 years)
To apply for this position or for more information, please contact: jennifer.barney@moffitt.org.
SOCRA Exp: 3/11/2021