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Review and validate clinical trial data, run diagnostics and reconciliations, generate and resolve queries, support database design and validation, ensure deliverables meet quality standards, assist in documentation and audits, and mentor junior staff within global FSP clinical programs.

Lead and support adjudication project management for clinical trials, overseeing project activities, team management, and ensuring compliance with operational standards.

Responsible for overseeing clinical trial site monitoring, ensuring compliance with protocols, managing site activities, and conducting training for new staff.

The Sr. CRA 2 will manage clinical site monitoring, ensure compliance with protocols, and support study integrity in oncology trials with required travel.