Clinical Trials Assistant — Patient-Centric Research Lead

ROVIA; West Monroe (LA); On-site; USD 42,000 - 56,000; Full time

Job summary

Rovia Clinical Research is seeking a Clinical Research Assistant to coordinate patient visits and support trials in line with ICH/GCP guidelines. The role collaborates with site teams to ensure accurate data capture, appropriate consent, and smooth visit flow.

Qualifications include a high school diploma, with a bachelor’s degree preferred, and experience with patient-facing activities. Proficiency in MS Office and EDC/CTMS is expected.

Qualifications

• High school diploma required; bachelor’s degree preferred.
• Experience with patient-facing activities is required.
• Phlebotomy or Medical Assistant certification preferred.

Responsibilities

• Coordinate and conduct patient visits per study protocol.
• Perform vitals, ECGs, specimen collection and phlebotomy as applicable.
• Ensure informed consent is properly obtained and documented.
• Maintain data quality and complete source documentation in EDC.
• Support monitoring visits, audits, and inspections.

Skills

Medical terminology

Clinical procedures

ICH/GCP

Organizational skills

Interpersonal communication

Multitasking

MS Office

EDC/CTMS

Education

High School Diploma

Bachelor’s degree preferred

Tools

Microsoft Office

EDC

CTMS

Job description

Rovia Clinical Research is seeking a Clinical Research Assistant to coordinate patient visits and support trials in line with ICH/GCP guidelines. The role collaborates with site teams to ensure accurate data capture, appropriate consent, and smooth visit flow.

Qualifications include a high school diploma, with a bachelor’s degree preferred, and experience with patient-facing activities. Proficiency in MS Office and EDC/CTMS is expected.