Ophthalmology Clinical Research Coordinator

Rovia Clinical Research; Jacksonville (FL); On-site; USD 45,000 - 65,000; Full time

Job summary

Rovia Clinical Research in Jacksonville, FL is seeking a Clinical Research Ophthalmology Assistant to coordinate and execute ophthalmology trials in line with ICH/GCP guidelines and sponsor requirements. You will partner with site teams to support study startup, enrollment, data quality, and study success.

Responsibilities include patient visits, retina imaging, CDVA and IOP assessments, ensuring proper informed consent, maintaining data integrity, and supporting monitoring visits and audits.

Qualifications

• 1 year as an Ophthalmic Technician, Ophthalmic Assistant, or Ophthalmic Photographer.
• Experience performing retina imaging required.
• Previous experience in clinical research preferred.

Responsibilities

• Conducts and coordinates patient visits in accordance with study protocols.
• Performs ophthalmology tasks such as retina imaging, CDVA, IOP, eye exams, etc.
• 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.
• Resolves data queries and ensures data integrity.
• 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.

Skills

Medical terminology

Clinical procedures

ICH/GCP

Regulatory knowledge

Organization

Communication skills

Multitasking

MS Office

EDC

CTMS

Independence

Teamwork

Confidentiality

Tools

retina imaging

Job description

Rovia Clinical Research in Jacksonville, FL is seeking a Clinical Research Ophthalmology Assistant to coordinate and execute ophthalmology trials in line with ICH/GCP guidelines and sponsor requirements. You will partner with site teams to support study startup, enrollment, data quality, and study success.

Responsibilities include patient visits, retina imaging, CDVA and IOP assessments, ensuring proper informed consent, maintaining data integrity, and supporting monitoring visits and audits.