Clinical Research Coordinator - Multisite Trials

Accel Research Sites; Charleston, Northern (SC, KY); On-site; USD 42,000 - 56,000; Full time

Job summary

Accel Research Sites is seeking a Clinical Research Coordinator to join the Operations team at Coastal Carolina Research Center in Charleston, SC. The CRC will ensure study execution in compliance with GCP, ICH, HIPAA, FDA regulations, and SOPs, coordinating with investigators and site staff.

The role involves patient screening, consent, follow-up visits, data entry in EDC, vitals/ECGs, basic lab work, and maintaining study logs and supplies.

Qualifications

• Minimum 1 year of clinical research or clinical experience.
• Medical/clinical credentials or degree required.
• Bi-lingual English/Spanish a plus.

Responsibilities

• Screen patients for study enrollment and obtain consent.
• Document in source charts and enter data in EDC.
• Obtain vitals, ECGs, and basic lab procedures per protocol.
• Maintain logs, schedules and study supplies.
• Coordinate with investigators and sponsor communications.

Skills

Clinical research

Bi-lingual English/Spanish

Strong communication

Attention to detail

Education

Associate’s degree

Medical Assistant diploma

LPN/LVN

EMT credential

Tools

Electronic health records

Microsoft Office

Job description

Accel Research Sites is seeking a Clinical Research Coordinator to join the Operations team at Coastal Carolina Research Center in Charleston, SC. The CRC will ensure study execution in compliance with GCP, ICH, HIPAA, FDA regulations, and SOPs, coordinating with investigators and site staff.

The role involves patient screening, consent, follow-up visits, data entry in EDC, vitals/ECGs, basic lab work, and maintaining study logs and supplies.