Teams at Fortrea

The Sr. CRA 2 is responsible for monitoring clinical trials, ensuring compliance with protocols, managing site activities, and training staff while traveling up to 60%.

Perform on-site and remote clinical site monitoring, ensure regulatory compliance and informed consent, review CRFs/EDC data, manage registries, report and follow up SAEs, support site initiation and close-out, train/co-monitor staff, and coordinate local project activities with frequent travel.

Lead and support clinical trials in Ophthalmology, overseeing monitoring and site management while ensuring adherence to protocols and data integrity.