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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.

As a Sr. CRA II, you will monitor clinical trial sites, ensuring compliance with protocols, managing data integrity, and reporting adverse events. You'll also assist with training and coordinate local projects as needed, requiring 5+ years of clinical monitoring experience, particularly in oncology.

The Sr. CRA II is responsible for monitoring clinical trials in oncology, ensuring protocol adherence, data integrity, and site management. This role includes coordinating clinical projects, conducting site visits, and training staff.

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

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