Location: Miami, FL
Job Type: Contract (15 Weeks)
Schedule: Monday – Friday, 8:30 AM – 5:00 PM
Pay: $32.00 – $43.00 per hour
Job Summary
We are seeking an experienced Senior Clinical Research Coordinator to support a busy clinical research team during a 15-week contract assignment. This role is responsible for coordinating all aspects of clinical research studies, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines while delivering exceptional patient care.
Responsibilities
- Coordinate and manage multiple clinical research studies from start-up through closeout.
- Screen, recruit, consent, and schedule study participants.
- Collect, document, and maintain accurate study data and source documentation.
- Ensure compliance with FDA, IRB, GCP, and sponsor requirements.
- Prepare for sponsor visits, monitoring visits, and audits.
- Coordinate study procedures, laboratory specimens, and investigational product accountability.
- Maintain regulatory binders and study documentation.
- Communicate effectively with investigators, sponsors, research staff, and participants.
- Assist with data entry, query resolution, and timely reporting of adverse events.
Qualifications
- 3+ years of clinical research coordination experience required.
- Experience coordinating industry-sponsored clinical trials.
- Strong knowledge of GCP, FDA regulations, and IRB processes.
- Excellent organizational, communication, and multitasking skills.
- Proficiency with electronic medical records (EMR) and clinical trial management systems is preferred.
- Current CPR certification and Clinical Research certification (CCRC or CCRP) are a plus.
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