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 documentation
- Managing site activities to ensure protocol adherence and patient safety
- Verifying informed consent and data integrity, including CRF review and SAE reporting
- Training and coordinating with site staff and acting as a local project or client contact
- Supporting 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 experience
- Comfort working in fast-paced, dynamic environments with changing priorities
- Strong teamwork, communication, and technology proficiency
Additional info:
- Requires 60-70% travel, including domestic and international sites
- Work environment involves office and travel; physical requirements include sitting, lifting, and computer use
- Benefits 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.