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Clinical Research Coordinator
Highly motivated and detail-oriented Clinical Research Coordinator with more than five years of experience in clinical trials and research operations. Skilled in coordinating and managing multiple clinical study protocols simultaneously, with experience overseeing more than four active protocols at one time. Bilingual professional with strong communication, multitasking, and interpersonal skills, capable of effectively collaborating with investigators, participants, sponsors, and multidisciplinary research teams. Experienced in EDC data entry and maintaining accurate clinical trial documentation.
Extensive knowledge of FDA regulations, ICH Good Clinical Practice (GCP) guidelines, HIPAA compliance, and clinical trial procedures. Proficient in participant recruitment, informed consent processes, patient monitoring, phlebotomy, data collection, EMR systems, and regulatory submissions. Proven ability to maintain accurate study records, ensure protocol compliance, and support the successful execution of clinical trials while prioritizing participant safety and data integrity.
Pay: $30.00 - $35.00 per hour
Work Location: In person
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