The Clinical Trials Office at Moffitt Cancer Center is looking for Study Activation Coordinators.
§ Responsible for initiating the startup of clinical research protocols and seeing them through to activation.
§ Will develop study related documents; anticipate potential obstacles to activation and pro-actively addressing obstacles to avoid delay.
§ Complete pre-site checklists provide information packets to sponsors and ensure timely distribution and return of pre-site paperwork and materials.
§ Follow up with internal and external customers for the duration of the activation process to ensure timely completion of tasks, including Investigational Drug Service (IDS), Clinical Trial Laboratory Core, Tissue Core, Regulatory, Budgets & Contracts and industry sponsors and vendors.
§ Attend pre-site visits, site initiation visits and other meetings/ conferences held periodically during the activation process; coordinate with the study team to make arrangements and document minutes.
Credentials and Qualifications:
§ Bachelor’s degree preferred with one (1) year experience in clinical trials (patient facing coordination, data management or other research coordination).
§ In lieu of a bachelor's degree an associate degree with three (3) years of experience in clinical trials (patient facing coordination, data management or other research coordination) may be considered.
§ One year in oncology preferred
§ One year of experience in clinical trial activation preferred
§ Clinical research certification preferred
*Please visit our website at www.moffitt.org/careers