Overview
Clinical Research Coordinator
Position: Clinical Research Coordinator (CRC)
Employment Type: Full-Time
About the Role
We are seeking an experienced and highly organized Clinical Research Coordinator to join our growing research team. The ideal candidate has experience coordinating industry-sponsored clinical trials while ensuring compliance with GCP, FDA regulations, and study protocols. This individual will play a key role in managing study operations and providing exceptional care to research participants.
Responsibilities
Coordinate and manage all aspects of clinical research studies from start-up through close-out.
Screen, recruit, and consent study participants.
Schedule and conduct study visits according to protocol.
Maintain accurate source documentation and electronic case report forms (eCRFs).
Ensure compliance with FDA regulations, ICH-GCP guidelines, and IRB requirements.
Communicate with sponsors, CROs, monitors, investigators, and study participants.
Prepare for and participate in monitoring, auditing, and regulatory inspections.
Process laboratory specimens and coordinate shipment when required.
Maintain regulatory binders and essential study documents.
Track study enrollment, participant retention, and protocol compliance.
Assist with adverse event reporting and protocol deviations.
Qualifications
Required:
Spanish / English bilingual
Minimum 1–2 years of clinical research coordinator experience
Experience coordinating pharmaceutical or device clinical trials
Strong knowledge of ICH-GCP and FDA regulations
Excellent organizational and communication skills
Ability to manage multiple studies simultaneously
Proficiency with EDC systems and Microsoft Office.
Preferred:
Experience with Phase II–IV clinical trials.
Experience working in outpatient clinical research.
We Offer
Competitive salary.
Paid time off.
Opportunities for professional growth.
Collaborative and supportive work environment.
Job Types: Full-time, Part-time, Contract, Temporary
Medical Specialty:
Work Location: In person
