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The role involves monitoring clinical trials, ensuring protocol adherence, managing data integrity, and training new employees, with significant travel required.

Lead and support clinical trials as a CRA II, ensuring compliance, monitoring sites, and managing data integrity with a focus on ophthalmology studies.

As a Senior Clinical Research Associate, you'll manage clinical trial sites, ensure compliance, perform monitoring, and coordinate projects. Involves onsite monitoring and patient safety. Requires significant oncology experience.

The Senior Clinical Research Associate will manage site monitoring, ensure compliance with protocols, assist with training, and report adverse events.