Clinical Research Coordinator: Patient-Centric Trials

Rovia Clinical Research; Georgia; On-site; USD 50,000 - 70,000; Full time

Job summary

Rovia Clinical Research in Georgia is seeking a Clinical Research Coordinator to coordinate and execute trials per protocol, ICH/GCP, and sponsor requirements. You will work closely with site teams to support study startup, enrollment, data quality, and overall study success.

The role requires familiarity with medical terminology, regulatory standards, and patient-facing activities. Strong organizational and communication skills, plus proficiency in EDC and CTMS, are essential for delivering

Qualifications

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

Responsibilities

• Coordinate patient visits according to study protocols.
• Perform clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
• Ensure informed consent is properly obtained and documented.
• Educate and guide participants through the study for a positive experience.
• Monitor subject safety, report adverse events, and escalate concerns as appropriate.
• Complete timely and accurate source documentation and EDC data entry.
• Resolve data queries and ensure data integrity.
• Maintain investigational product accountability and proper storage and handling.
• Prepare for and support monitoring visits, audits, and inspections.
• Collaborate with site staff and investigators to ensure protocol adherence and efficient visit flow.
• Perform other duties as assigned.

Skills

Medical terminology

Clinical procedures

ICH/GCP knowledge

Regulatory requirements

Organizational skills

Attention to detail

Interpersonal skills

Patient communication

Multitasking

MS Office

EDC

CTMS

Independent work

Team collaboration

Education

High school diploma

Bachelor's degree preferred

Tools

EDC systems

CTMS

Job description

Rovia Clinical Research in Georgia is seeking a Clinical Research Coordinator to coordinate and execute trials per protocol, ICH/GCP, and sponsor requirements. You will work closely with site teams to support study startup, enrollment, data quality, and overall study success.

The role requires familiarity with medical terminology, regulatory standards, and patient-facing activities. Strong organizational and communication skills, plus proficiency in EDC and CTMS, are essential for delivering