Clinical Research Coordinator: Lead Patient-Centric Trials

Accel Research Sites; Charleston (SC); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k with safe harbor match

Short/long-term disability

Job summary

Accel Research Sites seeks a Clinical Research Coordinator to ensure trial execution at our Coastal Carolina Research Center in Charleston, SC. You will support enrollment, patient visits, data entry in EDC, vital signs collection, and regulatory documentation under GCP and FDA regulations.

The role requires a Medical Assistant diploma or LPN/LVN/EMT or Associate degree with 1+ year in clinical research or clinical care, plus bilingual English/Spanish is a plus.

Qualifications

• Proficiency with computer applications such as Microsoft Office, email, electronic health records, and ability to type 40+ wpm.
• Must be able to perform basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy.
• Strong organizational skills, attention to detail, and good written/verbal communication.

Responsibilities

• Screening patients for study enrollment and obtaining patient consents.
• Conducting patient follow-up visits and ensuring accurate documentation.
• Entering data in EDC and responding to queries, obtaining vital signs and ECGs.
• Maintaining logs, chart filings, and study supplies; coordinating with team and sponsors.
• Ensuring HIPAA compliance and maintaining confidentiality of patient information.

Job description

Accel Research Sites seeks a Clinical Research Coordinator to ensure trial execution at our Coastal Carolina Research Center in Charleston, SC. You will support enrollment, patient visits, data entry in EDC, vital signs collection, and regulatory documentation under GCP and FDA regulations.

The role requires a Medical Assistant diploma or LPN/LVN/EMT or Associate degree with 1+ year in clinical research or clinical care, plus bilingual English/Spanish is a plus.