Clinical Research Coordinator - Patient-Centric Trials

ROVIA; Canton (GA); On-site; USD 52,000 - 72,000; Full time

Job summary

Rovia Clinical Research is seeking a Clinical Research Coordinator (CRC) to coordinate and execute clinical trials in line with ICH/GCP, study protocols, sponsor requirements, and Rovia SOPs. You will partner with site teams to support study startup, enrollment, data quality, and overall study success.

The ideal candidate has 1–3+ years in clinical research, strong knowledge of medical terminology, and excellent organizational and communication skills to ensure patient safety and data integrity

Qualifications

• High school diploma required; bachelor’s degree preferred.
• 1–3+ years of clinical research experience.
• Experience with patient-facing activities (phlebotomy, vitals, EKGs) strongly preferred.
• Strong knowledge of ICH/GCP and regulatory requirements.

Responsibilities

• Coordinate patient visits per study protocol.
• Perform clinical tasks such as vital signs, EKGs, samples collection and processing.
• Ensure informed consent is properly obtained and documented.
• Guide participants through the study to ensure a positive experience.
• Monitor subject safety and report adverse events.
• Complete timely source documentation and EDC data entry.
• Maintain investigational product accountability and storage.
• Prepare for monitoring visits, audits, and inspections.
• Collaborate with site staff and investigators to ensure protocol adherence.
• Perform other duties as assigned.

Skills

Medical terminology

Clinical procedures

ICH/GCP knowledge

Regulatory compliance

Organizational skills

Attention to detail

Interpersonal skills

Patient-facing communication

Multitasking

Team collaboration

Education

High school diploma

Bachelor’s degree preferred

Tools

EDC

CTMS

Microsoft Office

Job description

Rovia Clinical Research is seeking a Clinical Research Coordinator (CRC) to coordinate and execute clinical trials in line with ICH/GCP, study protocols, sponsor requirements, and Rovia SOPs. You will partner with site teams to support study startup, enrollment, data quality, and overall study success.

The ideal candidate has 1–3+ years in clinical research, strong knowledge of medical terminology, and excellent organizational and communication skills to ensure patient safety and data integrity