Clinical Research Associate II & Senior CRA - Ophthalmology & General Medicine

We are seeking experienced Ophthalmology Clinical Research Associates (Sr CRAs & CRA 1/2) to oversee and support clinical trial site monitoring and management. Key responsibilities include: Conducting routine monitoring, site close-outs, and maintaining study documentationManaging site activities to ensure protocol adherence and patient safetyVerifying informed consent and data integrity, including CRF review and SAE reportingTraining and coordinating with site staff and acting as a local project or client contactSupporting feasibility and registry management tasks Qualifications and skills: Degree or certification in a related health field (e.g., nursing licensure)1-3 years of clinical monitoring experienceComfort working in fast-paced, dynamic environments with changing prioritiesStrong teamwork, communication, and technology proficiency Additional info: Requires 60-70% travel, including domestic and international sitesWork environment involves office and travel; physical requirements include sitting, lifting, and computer useBenefits include health coverage, 401(k), PTO, and recognition awards This role emphasizes high-quality site monitoring, adherence to regulatory standards, and effective team collaboration in a fast-paced, technology-driven setting.