Clinical Research Coordinator

Clinical Research Coordinator Florida Clinical Trials Group Plantation, FL Job Details Full-time From $28 an hour 1 day ago Benefits Paid time off Qualifications Teamwork Clinical research English Research Clinical documentation Time management Full Job Description Role Description This is a full-time, on-site position for a Clinical Research Coordinator based in Plantation, Florida. The Clinical Research Coordinator will be responsible for coordinating and conducting clinical trials, managing study protocols and informed consent processes, and ensuring compliance with applicable regulatory requirements and GCP guidelines. Key responsibilities include participant recruitment and retention, scheduling study visits, collecting and maintaining accurate study documentation, and collaborating closely with investigators, sponsors, and clinical staff to ensure the successful execution of all assigned studies. Qualifications Strong understanding of clinical trial processes and study conduct Comprehensive knowledge of clinical research protocols, regulatory requirements, and Good Clinical Practice Previous experience in clinical research with direct involvement in clinical trials Proven ability to manage study activities, including participant recruitment, source documentation, data entry, and regulatory compliance Excellent organizational, time management, and communication skills Ability to work effectively in a fast-paced, collaborative, on-site environment Relevant background or equivalent experience in clinical research Certification as a Clinical Research Coordinator (CCRC) is preferred but not required

Pay:

From $28.00 per hour

Benefits:

Paid time off

Experience:

Clinical research: 1 year (Required)

Language:

English (Required)

License/Certification:

GCP Certificate (Preferred) IATA Dangerous Goods certification (Preferred)

Work Location:

In person