Ophthalmology Clinical Research Coordinator — Impactful Trials

Rovia Clinical Research; Jacksonville (FL); On-site; USD 52,000 - 72,000; Full time

Job summary

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

Responsibilities include coordinating patient visits, performing clinical tasks, ensuring informed consent, and maintaining source documentation. The role requires strong organization, communication, and a patient-focused approach at our Jacksonville sites.

Qualifications

• Minimum 2 years of clinical research experience.
• Bachelor’s degree in a related field preferred.
• Strong knowledge of ICH/GCP and regulatory requirements.
• Excellent organizational and patient-facing communication skills.

Responsibilities

• Coordinate patient visits per study protocol.
• Perform vital signs, EKGs, sample collection and processing as applicable.
• Ensure informed consent is properly obtained and documented.
• Educate participants and ensure a positive patient experience.
• Monitor subject safety and report adverse events.
• Maintain source documentation and EDC data entry.
• Support monitoring visits, audits, and inspections.
• Collaborate with site staff to ensure protocol adherence.

Skills

Medical terminology

ICH/GCP knowledge

Organizational skills

Interpersonal skills

Multitasking

MS Office

EDC proficiency

CTMS experience

Independent & collaborative

Patient confidentiality

Education

High school diploma

Bachelor's degree preferred

Tools

EDC

CTMS

MS Office

Job description

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

Responsibilities include coordinating patient visits, performing clinical tasks, ensuring informed consent, and maintaining source documentation. The role requires strong organization, communication, and a patient-focused approach at our Jacksonville sites.