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The Senior CRA will monitor clinical trial sites for compliance, conduct site visits, train site staff, and manage relationships with stakeholders in ophthalmology.

Oversee clinical trial operations, manage cross-functional teams, ensure regulatory compliance, and handle budgets and timelines in early phase oncology studies.

The Senior Clinical Research Associate will manage clinical trial activities, ensuring compliance with protocols and regulatory requirements while training site staff and maintaining data integrity.

The Senior CRA oversees clinical trial activities, ensuring compliance with protocols and regulatory standards, managing multiple sites, and providing training. Strong organizational and interpersonal skills are crucial.

The Senior CRA manages clinical trial activities, ensures compliance with protocols and regulations, and supports site staff to maintain trial integrity.

The candidate will manage site relationships, oversee clinical trial operations, ensure compliance, and collaborate with teams to optimize trial performance.

The Clinical Research Associate will conduct site visits, ensure protocol compliance, and review clinical data for trials. Responsibilities include collaborating with investigators and preparing study documentation.

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

The Senior Clinical Research Associate will manage clinical trials by conducting site visits, ensuring compliance, and contributing to study documentation.

As a Senior Clinical Research Associate, you will oversee clinical trials, ensuring adherence to protocols and regulatory standards, managing multiple sites, and collaborating with teams for data integrity and compliance.