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The Senior CRA 2 is responsible for site monitoring and management, ensuring regulatory compliance, data integrity, and overseeing clinical studies while traveling regionally for site visits.

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

Oversee Quality Control data tracking and reporting, collaborate with QC teams, maintain tracking systems, ensure compliance, and coordinate QC activities.

This role involves site monitoring and management for clinical studies, ensuring compliance with regulations and overseeing project plans. Responsibilities include data integrity checks, training staff, managing little projects, and maintaining communication with stakeholders.

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

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