COORD STUDY ACTIVATION SR at H. Lee Moffitt Cancer Center – Tampa, Florida

Job Summary:

The Coordinator Study Activation Senior (CSA Sr) is responsible for initiating the startup of a high volume of complex clinical research protocols and seeing them through to activation, in accordance with institutional and industry standards at Moffitt Cancer Center. The role works independently to facilitate and complete operational tasks associated with the startup of a large volume of clinical research protocols. This includes managing them through to activation at the cancer center in accordance with institutional and industry standards.

This position develops study related documents, anticipates potential obstacles to activation and proactively addresses them to avoid delay of clinical trial activation.

The incumbent is required to serve as a subject-matter expert and has a high proficiency regarding the knowledge of protocol requirements and good clinical practices as set forth by Federal regulations.

Minimum Experience Required:

Bachelor's degree with four (4) years of experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination) of which three (3) years in clinical trial activation is required.

**In lieu of a Bachelors degree:

• Associates degree with six (6) years of experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination) of which three (3) years in clinical trial activation is required OR
• High school diploma with eight (8) years of experience in clinical trials (as noted above) of which three (3) years required in clinical activation may be considered.

Must have one of the following certifications:

ACRP-CP/CCRC/CCRP