Ophthalmology Senior CRA Heavy, Impactful Trials
Listed on 2026-10-31
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Research/Development
Regulatory Compliance Specialist
Fortrea is seeking an experienced Senior Clinical Research Associate (CRA) with ophthalmology expertise to monitor trial sites across the United States. The role requires 3+ years of monitoring experience and 30-50% overnight travel to sites in major hubs in CA, TX, the South East and North East US.
You will manage site monitoring activities, ensure regulatory compliance, and support data integrity while collaborating with vendors and site staff in a fast-paced environment.
This is a great position to take on the Ophthalmology Senior CRA – Travel‑Heavy, Impactful Trials role at Fortrea.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Ophthalmology Senior CRA – Travel‑Heavy, Impactful Trials role in the description above.
We appreciate your interest in this position.
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