Clinical Research Coordinators assist with management of multiple trials and work directly with principal investigators. The Coordinators are responsible for overall management and implementation of clinical research protocols, ensuring compliance, efficiency, and the safety and well being of trial participants. Responsibilities include recruitment, consenting, screening and enrollment of study participants, coordinating appointments and visits, and management of study data.
Data Managers assist with the administrative aspects of study conduct including patient follow-up, clinical data and trial monitoring. |
Trial Administration