Research Associate I

Reviews medical records and conducts pre-screens and full screenings for study recruitment. Obtains informed consent from study participants, ensuring they understand the study procedures and requirements. Participate in recruiting efforts to enroll trial participants.Executes data collection procedure and assessments and assist with subject recruitment. Accurately enters data into electronic data capture systems and maintain data integrity. Reports adverse events in accordance with regulatory requirements and study protocols. Addresses and resolves data queries in a timely manner. Ensures compliance with regulatory requirements and guidelines associated with clinical trials.Participates in subject management, including phone calls and general coordination to schedule patients for study visits and follow-ups. Work closely with Principal Investigators (PIs), clinicians, and other research staff to facilitate study operations. Works both independently and as part of a team to achieve project goals. Performs administrative and coordinating tasks pertaining to study management.Other related functions as assigned.