COORD STUDY ACTIVATION I
Moffitt Cancer Center
- Tampa, FL
- Permanent
- Full-time
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.SummaryThe Coordinator Study Activation I (CSA I) is responsible for initiating the startup of clinical research protocols and seeing them through to activation, in accordance with institutional and industry standards at Moffitt Cancer Center. The incumbent is expected to work under moderate supervision and direction from the supervisor, manager and Principal Investigator to implement clinical research including administrative procedures for the successful conduct of clinical trials.The role will perform diverse administrative duties requiring analysis, sound judgment, and a knowledge of study conduct. This position has a good understanding of project management and possesses strong problem-solving and communication skills.The position develops study related documents, anticipates potential obstacles to activation and proactivly adressing them to avoid delay. This position will interact with leader of other functional areas within research administration which are involved in activation processes.Experience Required:Bachelors degree with one (1) year of experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination).**In lieu of a Bachelors degree:- An associate degree and three (3) years' experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination).- a high school diploma and five (5) years in clinical trials (patient facing coordination, data management, regulatory or other research coordination), may be considered.