What are the responsibilities and job description for the Clinical Research Coordinator (Full-Time / Part-Time) position at BIOMED RESEARCH INSTITUTE, INC?
Clinical Research Coordinator (Full-Time / Part-Time)
Location: Miami, Florida
Position Type: Full-Time or Part-Time
We are an established clinical research site seeking an experienced Clinical Research Coordinator (CRC) to join our team. The coordinator will assist with the day-to-day conduct of clinical trials and work closely with the Principal Investigator, research staff, sponsors, and CROs.
Candidates with prior clinical research experience who are organized, detail-oriented, and able to manage multiple studies are encouraged to apply.
- Coordinate clinical research studies in accordance with protocol, GCP, and regulatory requirements
- Screen and recruit potential study participants
- Schedule and conduct study visits
- Collect and document study data in Electronic Data Capture (EDC) systems
- Maintain regulatory documents and study files
- Communicate with sponsors, CROs, and study monitors
- Assist with query resolution and data clarification
- Ensure subject safety and protocol compliance
- Prior clinical research experience required
- Experience as a Clinical Research Coordinator preferred
- Knowledge of Good Clinical Practice (GCP) and clinical trial processes
- Experience with EDC systems (e.g., Medidata Rave or similar) preferred
- Strong organizational and communication skills
- Ability to manage multiple studies and work independently
Compensation will be based on experience.
Full-time or part-time opportunities available.
- Please submit your resume to: mgarcia@biomedresearchinst.com