Clinical Research Coordinator
- Miami, United States
Posted 25 days ago
About the role
Job Overview
We are seeking an experienced Clinical Research Coordinator to join our clinical research team. The ideal candidate must have at least 3 years of clinical research experience and be fully bilingual in English and Spanish. This role requires strong organization, patient communication skills, attention to detail, and the ability to support day-to-day study operations in compliance with protocol, GCP, and site procedures.
Responsibilities
- Coordinate daily clinical trial activities from screening through follow-up.
- Review protocols and support study startup, recruitment, prescreening, and scheduling.
- Obtain and document informed consent as delegated and permitted.
- Maintain accurate source documentation and study records.
- Enter and resolve data in EDC systems.
- Coordinate subject visits, labs, ECGs, vitals, questionnaires, IP accountability support, and study-specific procedures.
- Communicate with participants, caregivers, sponsors, CROs, monitors, vendors, and investigators.
- Prepare for monitoring visits and assist with query resolution.
- Track recruitment, enrollment, visit windows, deviations, and study action items.
- Ensure study activities follow GCP, protocol requirements, and site SOPs.
Requirements
- Minimum 3 years of experience as a Clinical Research Coordinator or similar clinical research role.
- Fluent bilingual communication skills in English and Spanish, spoken and written.
- Experience with sponsor/CRO monitoring visits, EDC systems, source documentation, and regulatory binders.
- Strong knowledge of GCP and clinical trial conduct.
- Excellent organization, follow-up, and time-management skills.
- Comfortable communicating with patients and study participants.
- Ability to work on-site and manage multiple studies/tasks.
- Proficiency with Microsoft Office or Google Workspace.
Preferred Qualifications
- Experience in CNS, psychiatry, neurology, metabolic, nephrology, or outpatient studies.
- Phlebotomy, ECG, vitals, lab processing, or IATA training.
- CCRC certification or other clinical research certification.
- Experience with recruitment and prescreening workflows.
Compensation
Depending on experience.
Schedule
Monday to Friday, [8am to 5 pm]. Occasional flexibility may be required based on study visits.
How to Apply
Please submit your resume through Indeed. Qualified candidates may be contacted for a phone screening and interview.
Pay: Up to $72,000.00 per year
Work Location: In person