Find & Apply For Clinical Research Coordinator Jobs in Coral Gables, Florida

Clinical Research Coordinator Highly motivated and detail-oriented Clinical Research Coordinator with more than 1 year 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. Ensures all deviations, violations, AEs, and SAEs are captured, recorded, followed, and reported to Sponsor/IRB in a timely manner. 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. Consents study participants following the Site's SOPs. 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. Confirm with the Front desk personnel, Laboratory technicians, and Assistant CRC, subjects scheduled for the following day.

Education and Experience:

1+ years of Clinical Research experience preferred.

Skills :

MUST BE BILINGUAL

Pay:

$20.00 - $25.00 per hour Expected hours: 40.0 per week

Work Location:

In person