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

We are seeking experienced Ophthalmology (Sr CRAs & CRA 1/2) to lead and support clinical trial monitoring within a Full Service Outsourcing team. This role involves approximately 60-70% travel, with responsibilities across site management, study monitoring, data integrity, and regulatory compliance. Key responsibilities include: Conducting routine and close-out site visits, maintaining study files, and liaising with vendorsEnsuring proper site staff training and adherence to protocol and regulatory standardsVerifying informed consent, monitoring data accuracy, and managing registry activitiesHandling SAE reporting, CRF review, query resolution, and assisting in staff trainingCoordinating clinical projects and acting as a local contact as needed Qualifications and skills: Degree or certification in health-related fields (e.g., nursing license)1-3 years of clinical monitoring experienceStrong teamwork, communication, adaptability in fast-paced, evolving environmentsProficiency with electronic data collection and regulatory requirements Additional information: Work environment includes office and travel to client/site locationsPhysical requirements include sitting, lifting, computer use, and occasional movementBenefits include health insurance, 401(k), PTO, and employee recognition