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Oversee and manage clinical trial activities, ensuring compliance with protocols and regulations, while mentoring site staff and maintaining data integrity.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations, mentoring staff, and managing site performance for successful trials.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; contribute to study documentation and clinical study reports.

As a Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulations, and provide support to trials.

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with sites; review data and support study documentation.

The Jr. Clinical Supply Manager coordinates logistics, manages shipments, supports supply chain strategies, and maintains inventory records to ensure efficiency.

The Senior Biostatistician II will oversee clinical trials, manage statistical deliverables, lead client interactions, and mentor junior staff.

The Feasibility Principal Analyst leads feasibility strategy and analysis for clinical studies, synthesizing data to inform study planning and enrollment decisions while mentoring junior team members.