GENERAL SUMMARY/ OVERVIEW STATEMENT:
The Clinical Research Data Coordinator II (CRDC II) works independently under general supervision to enroll eligible patients to clinical research protocols and manage data collection and regulatory submissions for multiple cancer studies. The CRDC II will be the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting. The CRDC II will have experience with institutional and federal regulations governing clinical research. The position involves a high volume of data abstraction and data entry. This position does not include any direct patient contact.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
The CRDC II will perform the following data management duties independently under general supervision by the Clinical Research Manager:
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