Clinical Research Coordinator - Impactful Trials

Rovia; Bastrop (LA); On-site; USD 52,000 - 73,000; Full time

Job summary

Rovia Clinical Research is seeking a Clinical Research Coordinator (CRC) to coordinate and execute clinical trials per study protocols, ICH/GCP guidelines, and SOPs. The role partners with site teams to support study startup, enrollment, data quality, and overall study success.

Responsibilities include coordinating patient visits, performing clinical tasks, ensuring informed consent, and maintaining source documentation and EDC data entry.

Qualifications

• High school diploma required; bachelor’s degree preferred.
• At least 1 year of clinical research experience.
• Experience with patient-facing activities (phlebotomy, vitals, EKGs) preferred.

Responsibilities

• Coordinates patient visits per study protocols and GCP guidelines.
• Ensures informed consent is properly obtained and documented.
• Maintains study documentation and data entry accuracy (EDC).
• Supports site startup, enrollment, data quality, and study success.
• Assists with monitoring visits, audits, and inspections.
• Protects patient confidentiality and safety at all times.

Skills

Medical terminology

ICH/GCP

Organization

Interpersonal skills

Multitasking

Microsoft Office

EDC

CTMS

Independence

Confidentiality

Education

High school diploma required

Bachelor's degree preferred

Tools

Microsoft Office

EDC

CTMS

Job description

Rovia Clinical Research is seeking a Clinical Research Coordinator (CRC) to coordinate and execute clinical trials per study protocols, ICH/GCP guidelines, and SOPs. The role partners with site teams to support study startup, enrollment, data quality, and overall study success.

Responsibilities include coordinating patient visits, performing clinical tasks, ensuring informed consent, and maintaining source documentation and EDC data entry.