Jobs at Fortrea

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

The role involves monitoring clinical trial sites, ensuring protocol adherence, reporting serious adverse events, and training new staff, with 5+ years' experience required.

The Sr. CRA 2 will monitor clinical trial sites, manage study compliance, ensure data integrity, and oversee patient safety in oncology studies, requiring strong clinical judgment and teamwork.

The Sr. CRA 2 will monitor clinical trials, manage study sites, ensure regulatory compliance, and assist with training and data integrity verification.

Responsible for monitoring clinical trials, ensuring compliance with protocols, data integrity, site management, and training new employees, with significant oncology experience required.

Lead statistical design, analysis, and interpretation for complex oncology clinical trials (including NDA-level programs). Develop and review SAPs, perform complex analyses and sample size calculations, support DMCs, prepare protocol and CSR statistical sections, generate randomization schedules, manage project timelines/resources, mentor junior staff, represent the department in audits and bids, and present results internally and externally. Remote work with minimal travel (~5%).

Responsible for site monitoring, ensuring protocol compliance, data integrity, and training new employees for clinical trials in oncology.

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.