Study Coordinator

The Study Coordinator position at Howard University is a full-time role focused on coordinating study patients within the Clinical Trials Unit. The primary responsibility of the Study Coordinator is to execute tasks as required by the study protocols, ensuring that all procedures are followed accurately and efficiently. This role involves significant interaction with various stakeholders, including physicians, hospital and university officials, patients, and their caretakers. The Study Coordinator must maintain a thorough understanding of the study protocols and evaluate candidates for eligibility, ensuring that informed consent is obtained from patients or their legal guardians before any research-related activities commence. In addition to patient coordination, the Study Coordinator is responsible for scheduling tests and appointments, managing prescriptions for study medications, and providing clear instructions regarding medication dosing. The role also includes monitoring patient compliance with study protocols, identifying abnormal laboratory results, and ensuring that necessary follow-up evaluations are conducted. Accurate documentation is crucial, as the Study Coordinator must complete case report forms and maintain source documentation for each study participant. This position requires timely responses to data inquiries and the completion of Serious Adverse Event Reports as per regulatory requirements. The Study Coordinator will also participate in planning and implementing special events within the research unit, such as symposia or conferences, and may assist with grant writing as assigned. If the incumbent holds a valid Physician Assistant or Nurse Practitioner license, they may perform clinical duties as directed by the Principal Investigator. Overall, this role is integral to the success of clinical trials at Howard University, contributing to the institution's mission of advancing health and wellness through research and education.