Clinical Research Coordinator - Impactful Trials & Growth

Accel Research Sites; North Charleston (SC); On-site; USD 42,000 - 65,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k) with match

Disability insurance

Job summary

Alcanza is seeking a Clinical Research Coordinator to ensure study execution in line with GCP, ICH, HIPAA, FDA, and SOPs. The CRC will screen patients, obtain consent, perform follow‑ups, and manage source documentation at the Charleston site.

The role involves data entry in EDC, collecting vital signs/ECGs, coordinating visits, and maintaining study logs. Strong communication and multitasking are essential, with bilingual ability valued.

Qualifications

• Minimum qualifications include a Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree.
• Experience in clinical research or clinical settings for 1 year is required.
• Bilingual English/Spanish is a plus.

Responsibilities

• Screening patients for study enrollment and obtaining informed consent.
• Conducting patient follow‑up visits and recording data in EDC.
• Handle vital signs, ECGs, and basic lab procedures per protocol.
• Maintain logs and source documentation, ensure HIPAA compliance.

Skills

Clinical procedures

Bilingual English/Spanish

Strong communication

Multitasking

Education

Medical Assistant diploma

Associate degree

LPN/LVN

EMT credential

Tools

Microsoft Office

Electronic health records

Web applications

Job description

Alcanza is seeking a Clinical Research Coordinator to ensure study execution in line with GCP, ICH, HIPAA, FDA, and SOPs. The CRC will screen patients, obtain consent, perform follow‑ups, and manage source documentation at the Charleston site.

The role involves data entry in EDC, collecting vital signs/ECGs, coordinating visits, and maintaining study logs. Strong communication and multitasking are essential, with bilingual ability valued.