Assistant Clinical Research Coordinator

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Assistant Clinical Research Coordinator at University of California, Irvine

Orange, CA | Full Time
$74k-100k (estimate)
2 Months Ago
Job Opening ID. 63229. Reports To. Clinical Research Manager and the Director of Clinical Research Operations. Working Title. Assistant Clinical Research Coordinator. Department. UCI Ctr for Clinical Research. Bargaining Unit. RX. FLSA. Non-Exempt. Payroll Job Code. 009336. Job Location. UCI Campus- Irvine. Percent of Time. 100%. Work Schedule. 8-5, M-F. Employee Class. Career. Position Summary. The UCI Center for Clinical Research (CCR) is drive...

Assistant Clinical Research Coordinator at University of California - Los Angeles Health

Los Angeles, CA | Full Time
$59k-79k (estimate)
4 Months Ago
Description. The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. In this role, you will perform necessary tasks to assist in managing projects and prioritizing work to meet necessary deadlines. You will provide support in planning and organizing necessary tasks to ensure a...

Assistant Clinical Research Coordinator at UCLA Health Careers

Los Angeles, CA | Full Time
$74k-101k (estimate)
7 Months Ago
Description. The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. In this role, you will perform necessary tasks to assist in managing projects and prioritizing work to meet necessary deadlines. You will provide support in planning and organizing necessary tasks to ensure a...

Assistant Clinical Research Coordinator at Apex Research Group

Fair Oaks, CA | Full Time
$62k-82k (estimate)
9 Months Ago
Assistant Clinical Research Coordinator (entry-level position, 0-1. year experience in Clinical Research preferred). Duties. Plan, execute, and assure quality of assigned clinical trials. Perform the Informed Consent Discussion. Complete and/or assist with assigned protocol procedures, chart preparation and recording. completed case report forms. conduct medical histories, and vital signs. Schedule protocol procedures and visits. Assist in partic...
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