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As a Senior Clinical Research Associate, you will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with investigators. Traveling 60% of the time is required.

The Senior Clinical Research Associate will manage site activities and ensure compliance during Oncology clinical trials, focusing on data integrity and subject safety.

Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.

The Senior Clinical Research Associate will monitor cardiovascular devices, ensuring compliance with FDA regulations and managing study communication, while travelling regionally up to 65%.

The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

As a Senior CRA, you will monitor clinical trial sites, ensure compliance with regulations, manage site performance, and train staff to maintain trial standards.

As a Clinical Research Associate II, you will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff.

The Senior CRA will oversee clinical trial activities, ensuring adherence to protocols and regulatory requirements while managing multiple sites and projects.

The Clinical Research Associate will manage clinical trial processes including site visits, data integrity, and prepare study documentation to ensure compliance and patient safety.

The Clinical Research Associate will manage clinical trials, ensure compliance and data integrity, and collaborate with site staff and investigators.