Clinical Research Coordinator

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

About Us

At Rovia Clinical Research, we're on a mission to bring innovative treatments to patients, improving the health and lives of our local patient communities. We believe in building a workplace where people feel supported, valued, and excited to grow their careers. Whether you're just starting out or looking for a new path, you'll be part of a team that truly works together and makes an impact. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability.

Position Summary

The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

Key Responsibilities

• Conducts and coordinates patient visits in accordance with study protocols.
• Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
• Ensures informed consent is properly obtained and documented.
• Educates and guides participants through the study, ensuring a positive patient experience.
• Monitors subject safety, reports adverse events, and escalates concerns as appropriate.
• Completes timely and accurate source documentation and EDC data entry.
• Resolves data queries and ensures data integrity.
• Maintains investigational product accountability and proper storage and handling.
• Prepares for and supports monitoring visits, audits, and inspections.
• Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
• Perform other duties as assigned.

Skills/Abilities

• Strong knowledge of medical terminology and clinical procedures.
• Understanding of ICH/GCP and regulatory requirements.
• Excellent organizational skills and attention to detail.
• Strong interpersonal and patient-facing communication skills.
• Ability to multitask and manage competing priorities in a fast-paced environment.
• Proficiency in Microsoft Office, EDC, and CTMS applications.
• Ability to work both independently and collaboratively.
• High level of professionalism and commitment to patient confidentiality.

Education / Experience

• High school diploma required, bachelor's degree in related field preferred.
• 1-3 years of clinical research experience.
• Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred.