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As a Clinical Research Associate, you'll conduct clinical trials, ensuring protocol compliance and data integrity while collaborating with site staff and investigators.

As a Clinical Research Associate, you will monitor clinical trials, ensure protocol compliance, collaborate with site staff, and maintain data integrity.

The Senior Biostatistician I will lead early phase clinical trials, provide statistical inputs for protocols and reports, and mentor junior statisticians.

The Lead CRA manages clinical trial sites, ensures compliance with regulations, mentors CRAs, and oversees data integrity. Responsibilities include site management, issue resolution, and collaboration with cross-functional teams.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring compliance and data integrity, while collaborating with site staff and preparing study documentation.

As a Clinical Research Associate, conduct site visits, ensure compliance and safety, collaborate with staff, and review clinical data documentation.

The Senior Clinical Research Associate will manage clinical trials, ensure compliance, analyze data, and collaborate with study personnel while traveling extensively.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with site staff and investigators.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and study protocols, mentoring CRAs, and ensuring data integrity and patient safety.

As a Senior Clinical Trial Manager, you will manage clinical trial operations, oversee budgets, develop monitoring plans, drive enrollment, and foster relationships with stakeholders.