Clinical Research Coordinator — Fast-Paced, Data-Driven Trials

Folio Clinical Research; Charlotte (NC); On-site; USD 33,000 - 44,000; Full time

Job summary

Folio Clinical Research in Charlotte, NC is seeking a Clinical Research Coordinator to support trial operations, data entry, patient pre-screening, and scheduling. You will work closely with investigators, staff, and sponsors to ensure compliant, efficient study execution.

The role emphasizes regulatory adherence (GCP/IRB), data management, and collaboration with the site team to drive study success and quality across multiple trials.

Qualifications

• Bachelor's degree in science or health-related field.
• Knowledge of GCP/IRB regulatory requirements.
• Experience with EDC, CTMS and eTMF systems.

Responsibilities

• Assist PI/SI and CRCs with trial tasks including data entry and patient scheduling.
• Support site setup, equipment calibration, and supply orders for study readiness.
• Attend SQVs, SIVs, monitoring visits and coordinate FPV/FPS/FPE readiness.
• Ensure regulatory compliance and data integrity across trials.
• Assist with trial management system expansion and technology adoption.

Skills

Attention to detail

Communication

Time management

Team collaboration

Data management

Education

Bachelor's degree in science or health-related field

Tools

EDC

CTMS

eTMF

IXRS

RTSM

Job description

Folio Clinical Research in Charlotte, NC is seeking a Clinical Research Coordinator to support trial operations, data entry, patient pre-screening, and scheduling. You will work closely with investigators, staff, and sponsors to ensure compliant, efficient study execution.

The role emphasizes regulatory adherence (GCP/IRB), data management, and collaboration with the site team to drive study success and quality across multiple trials.