The ICE-T Data Management program in the Clinical Trials Office is looking for a Study Activation Coordinator II.
Responsible for initiating the startup of clinical research protocols and seeing them through to activation.
Develops study-related documents, anticipates potential obstacles to activation.
Creates multiple study-related documents including in-service sheets, orders, eligibility checklists, Delegation of Authority (DOA) logs, Adverse Event (AE) logs.
Credentials and Qualifications:
Associate’s degree with four(4) years of experience in clinical trials(patient facing coordination, data management, regulatory or other research coordination, preferably in oncology)
Bachelor's degree preferred with two (2) years of experience in clinical trials(patient facing coordination, data management, regulatory or other research coordination, preferably in oncology)
CCRP/CCRC or equivalent preferred.
To create a Moffitt culture of diversity and inclusion as we strive to contribute to the prevention and cure of cancer.
Moffitt Cancer Center is recognized as the model wherein the diversity of our employees and communities is valued and supported as essential components to contributing to the prevention and cure of cancer.
The cancer center is an equal opportunity employer. It is the policy of the cancer center to prohibit unlawful discrimination and harassment of any type and to afford equal employment opportunities to workforce members and applicants, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, marital status, disability, genetic information, veteran’s status or any other characteristic protected by federal, state or local law.