Description:
Job Description Under the direct supervision of the study team and research leadership, assists in coordinating the details of the study and documentation concerning study protocols, patient scheduling, retrospective & prospective chart work, data collection, data entry, data management, follow-up information, and compliance with federal, state, sponsor, and institutional guidelines. Overview for the Clinical Data Associate I: The CDA I provides data management support for clinical trials. The
Jul 13, 2025;
from:
dice.com