Clinical Research Coordinator 1 - OLOL

Job description

The Clinical Research Coordinator I (CRC I) is responsible for assisting with the day-to-day activities of clinical research studies under the supervision of the Principal Investigator (PI) or Clinical Research Nurse and in accordance with Good Clinical Practice (GCP) guidelines, FDA regulations, and institutional policies. The CRC I is responsible for assisting with study operations, participant recruitment, and data management contributing to the overall success of clinical trials. This is an entry-level role for individuals seeking to develop their career in clinical research. #CB Program Management: 1. Assist in the coordination of clinical research studies, including study start-up, execution, and close-out activities. 2. Ensure all study activities are conducted in compliance with the study protocol, GCP, and relevant regulatory guidelines. 3. Screen, recruit, and enroll study participants according to the inclusion/exclusion criteria outlined in study protocols and as instructed by the PI. 4. Obtain informed consent from study participants and ensure their understanding of study procedures. 5. Conduct basic clinical assessments such as taking vitals and or administering ques...