Comprehensive EyeCare Partners is one of the nations largest vision care management service organization. CompEye is focused on providing best-in-class, full-spectrum practice management and administrative services to its affiliated physicians and practices in support of their mission to deliver clinical excellence. Our mission is to build nation’s preeminent eye care services company by partnering with world class physicians, driving superior clinical and surgical outcomes, and optimizing the patient experience.
Enlist, maintain, and assure protocol compliance for all patients in clinical trials.
Collaborate with physicians to determine patient eligibility for clinical trials.
Ensure site research quality by practicing compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP), and applicable regulations.
Coordinate patient care in compliance with protocol requirements, including disbursement of investigational drugs and patient teaching.
Review patients for changes in condition, adverse events, protocol compliance, and response to study drug, thoroughly documenting all findings.
Provide a safe environment for patients, families, and clinical staff, adhering to federal, state, and professional regulatory standards.
Assist the research team in various study activities such as recruitment, screening, study visits, and termination.
Enter study data into the data system such as the Case Report Form per protocol requirements.
Perform assigned work safely, adhering to established departmental safety rules and practices; report any unsafe activities or conditions promptly to the supervisor.
