Senior Ophthalmology Trials Coordinator - Jacksonville

ROVIA; Jacksonville (FL); On-site; USD 70,000 - 90,000; Full time

Job summary

Rovia Clinical Research seeks a Senior Clinical Research Coordinator to coordinate ophthalmology clinical trials across Jacksonville sites. You will manage patient visits, collect samples, ensure consent, and maintain data integrity per ICH/GCP standards.

You will monitor safety, support monitoring visits, and collaborate with site staff to ensure protocol adherence and efficient visit flow, while maintaining patient confidentiality and quality documentation.

Qualifications

• High school diploma required; bachelor’s degree preferred.
• 3+ years of clinical research experience.

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

Medical terminology

ICH/GCP knowledge

Organizational skills

Interpersonal communication

Multitasking

Patient confidentiality

Education

High school diploma

Bachelor’s degree preferred

Tools

Microsoft Office

EDC

CTMS

Job description

Rovia Clinical Research seeks a Senior Clinical Research Coordinator to coordinate ophthalmology clinical trials across Jacksonville sites. You will manage patient visits, collect samples, ensure consent, and maintain data integrity per ICH/GCP standards.

You will monitor safety, support monitoring visits, and collaborate with site staff to ensure protocol adherence and efficient visit flow, while maintaining patient confidentiality and quality documentation.