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The Sr. CRA II will oversee study site monitoring, ensure protocol compliance, manage data integrity, and coordinate clinical projects while traveling frequently.

Oversee clinical trial operations, manage budgets, negotiate contracts, ensure compliance, and collaborate with teams to achieve trial objectives.

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%.

Senior Clinical Research Associate responsible for site monitoring, data integrity, SAE reporting, CRF review, site management and feasibility, and coordinating local project activities for oncology studies. Requires heavy travel and training/co-monitoring support duties.

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