Optometry Clinical Research Coordinator

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our optometry-focused research team in Johns Creek, GA . This role is ideal for someone passionate about advancing eye care through clinical studies and patient-focused research.

Job Description

• Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Travel (approximately 0%) domestic and / or international.
• Communicate protocol requirements to clinical and laboratory staff.
• Participate in the early planning phases of clinical study by providing assistance in the preparation of study proposal timelines, scheduling and other study requirements as appropriate.
• Evaluate, coordinate, and ensure the completion of all protocol related tasks to include : design of procedural timeline; design of forms and source documents used in the clinical research process; maintain clinical study enrolment log; and assist Data Coordinators regarding CRFs and regulatory documents.
• Obtain input of the clinical staff as it pertains to the development of the source documents, forms, and procedural timelines.
• Coordinate with Study or Project Manger to ensure appropriate timelines are being met as per contractual obligations.
• Attend meetings with Sponsors for assigned protocol.
• Participate in meetings to include (pre-planning and clinical tracking).
• Assure resolution of all Quality Control discrepancies related to data and research documents.
• Lead and coordinate interdepartmental start up meetings, and mock runs to ensure that all clinical staff is trained on protocol procedures.
• Coordinates with Screening and Recruitment to maintain timely execution of study enrolment.
• Coordinate and ensure with Data Management to ensure timely submission of regulatory documents to IRB and CRF completion.
• Coordinate with Study or Project Manager to provide requested information for interim status report to sponsor.
• Carry out clinical study directives from the Principal / Sub Investigator.
• Understand protocol requirements and communicate those requirements to applicable staff.
• To undertake other reasonably related duties as may be assigned from time to time.

What you will be doing

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