Ophthalmology Clinical Trials Coordinator

Universal Axon Clinical Research, LLC; Anniston (AL); On-site; USD 42,000 - 64,000; Full time

Job summary

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

Responsibilities include coordinating visits, performing clinical tasks, ensuring proper consent, monitoring safety, and maintaining accurate documentation. A strong focus on patient experience and regulatory compliance is essential.

Qualifications

• Must have a high school diploma.
• Current MA certification or nursing licensure (LPN, RN) preferred.
• Strong knowledge of medical terminology and clinical procedures.
• Familiarity with ICH/GCP and regulatory requirements.

Responsibilities

• Coordinates patient visits per study protocols.
• Performs vital signs, EKGs, specimen collection and processing as applicable.
• Ensures informed consent is properly obtained and documented.
• Educates and guides participants through the study to ensure a positive experience.
• Monitors subject safety and reports adverse events as appropriate.
• Maintains source documentation and EDC data entry.
• Prepares for and supports monitoring visits, audits and inspections.
• Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
• Performs other duties as assigned.

Skills

Medical terminology

ICH/GCP knowledge

Organizational skills

Interpersonal communication

Multitasking

Collaboration

Patient confidentiality

Education

High School Diploma

MA certification

Nursing licensure (LPN, RN)

Tools

Microsoft Office

EDC

CTMS

Job description

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

Responsibilities include coordinating visits, performing clinical tasks, ensuring proper consent, monitoring safety, and maintaining accurate documentation. A strong focus on patient experience and regulatory compliance is essential.