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 vendors
- Ensuring proper site staff training and adherence to protocol and regulatory standards
- Verifying informed consent, monitoring data accuracy, and managing registry activities
- Handling SAE reporting, CRF review, query resolution, and assisting in staff training
- Coordinating 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 experience
- Strong teamwork, communication, adaptability in fast-paced, evolving environments
- Proficiency with electronic data collection and regulatory requirements
Additional information:
- Work environment includes office and travel to client/site locations
- Physical requirements include sitting, lifting, computer use, and occasional movement
- Benefits include health insurance, 401(k), PTO, and employee recognition