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