Clinical Research Coordinator

Rovia Clinical Research; Canton (GA); On-site; USD 55,000 - 75,000; Full time

Job summary

Rovia Clinical Research is hiring a Clinical Research Coordinator (CRC) to coordinate and execute clinical trials in alignment with study protocols and ICH/GCP guidelines. You will partner with site teams to support startup, enrollment, data quality, and study success.

The role requires strong medical terminology knowledge, regulatory awareness, and exceptional organizational and patient-facing communication skills. Prior experience with phlebotomy, EKGs, and data entry is preferred.

Qualifications

• High school diploma required; bachelor’s degree preferred.
• 1–3+ years of clinical research experience.
• Experience with patient-facing activities (phlebotomy, vital signs, EKGs) strongly preferred.

Responsibilities

• Coordinate and execute clinical trials per study protocols and ICH/GCP.
• Perform clinical tasks including vital signs, EKGs, phlebotomy, and specimen handling as applicable.
• Ensure informed consent is properly obtained and documented.
• Support study startup, enrollment, data quality, and study success.
• Monitor subject safety and report adverse events; escalate concerns as needed.
• Complete source documentation and EDC data entry accurately.
• Maintain investigational product accountability and storage.
• Prepare for and support monitoring visits, audits, and inspections.
• Collaborate with site staff to ensure protocol adherence and efficient visit flow.

Skills

Clinical terminology

ICH/GCP knowledge

Organizational skills

Patient communication

Multitasking

MS Office / EDC / CTMS

Team collaboration

Confidentiality

Education

High school diploma

Bachelor’s degree preferred

Tools

Microsoft Office

EDC

CTMS

Job description

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.
• 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.