Remote Ophthalmology Senior CRA II for Impactful Trials

Fortrea; Connecticut; On-site; USD 125,000 - 142,000; Full time

Job summary

Expect 30-50% overnight travel, on-site monitoring, SAE reporting, and collaboration with study teams. Ideal candidates thrive in fast-paced environments and adapt to changing priorities while maintaining quality.

Qualifications

• Minimum 4+ years of clinical monitoring experience in ophthalmology trials.
• Oncology experience and early-phase exposure preferred.
• Ability to travel 30-50% overnight.

Responsibilities

• Oversee all aspects of site monitoring, including routine visits, close-out, and initiation visits.
• Ensure protocol compliance, informed consent, and data integrity on CRFs.
• Coordinate registry management and feasibility work as needed.
• Conduct CRF review, query generation, and data quality checks.
• Assist with training of new staff and liaise with vendors as assigned.
• Travel and site coordination as Local Project Coordinator or client contact.

Skills

Clinical Monitoring

Oncology experience

Team collaboration

Education

University degree or nursing licensure

Job description

Expect 30-50% overnight travel, on-site monitoring, SAE reporting, and collaboration with study teams. Ideal candidates thrive in fast-paced environments and adapt to changing priorities while maintaining quality.