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The Feasibility Informatics Manager leads clinical project feasibility, providing strategic input and delivering feasibility studies on time and on budget, collaborating with cross-functional teams to ensure high-quality outcomes.

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

Oversee site contracts for clinical studies, manage contract development, collaborate with teams, ensure financial management, and mentor others.

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

The Site Specialist II role involves supporting regulatory documentation, ensuring compliance for site activation, and collaborating with stakeholders for optimal study performance.

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

The Senior Clinical Research Associate will oversee clinical trial activities, ensuring adherence to protocols, conduct site visits, and manage data integrity while providing support and training to site staff.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and protocols while mentoring CRAs and collaborating with teams to execute trials effectively.

The Senior CRA ensures quality execution at clinical trial sites, conducts oversight visits, supports compliance, and enhances quality performance across studies.

Lead biostatistical components in clinical trials, oversee statistical activities, mentor junior statisticians, and ensure regulatory compliance.