Senior Ophthalmology CRA - Remote, Fast-Paced Trials

Fortrea; Yorktown (VA); Remote; USD 130,000 - 142,000; Full time

Job summary

Fortrea is seeking a Sr. CRA with ophthalmology monitoring expertise to join our FSP team. You will monitor clinical sites, ensure data integrity, and manage regulatory compliance while traveling up to 50% across the US.

The role requires a university degree or allied health certification and at least 3 years of clinical monitoring experience. Strong team collaboration and adaptability are essential for success in a fast-paced, technology-driven environment.

Qualifications

• University or college degree or certification in a related allied health profession (e.g. nursing licensure)
• 3+ years of Clinical Monitoring experience
• 30-50+% overnight travel
• Ophthalmology experience

Responsibilities

• Responsible for all aspects of site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of visits and liaising with vendors
• Responsible for all aspects of site management as prescribed in project plans
• General On-Site Monitoring
• Ensure protocol staff have proper materials and instructions to safely enter patients into the study
• Ensure informed consent procedures and protocol requirements are followed per regulatory requirements
• Verify data integrity on CRFs and other data collection tools; monitor data for missing or implausible data
• Support registry management and feasibility work as requested
• Complete SAE reporting and narratives with follow-up
• CRF review, query generation and resolution per guidelines
• Assist with training of new employees (e.g., co-monitoring)
• Coordinate designated clinical projects as Local Project Coordinator and act as client contact when assigned
• Perform other duties as assigned by management

Skills

Clinical monitoring

Ophthalmology experience

Education

Bachelor's degree or higher in related allied health field

Job description

Fortrea is seeking a Sr. CRA with ophthalmology monitoring expertise to join our FSP team. You will monitor clinical sites, ensure data integrity, and manage regulatory compliance while traveling up to 50% across the US.

The role requires a university degree or allied health certification and at least 3 years of clinical monitoring experience. Strong team collaboration and adaptability are essential for success in a fast-paced, technology-driven environment.