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The Clinical Quality Assurance Specialist ensures compliance with GCP standards through audit support, risk management, data integrity, and cross-functional collaboration in clinical trials.

The biostatistics manager will lead statistical input for clinical studies, collaborate with various teams, ensure deliverable integrity, and oversee CROs' work.

The Manager of Statistical Programming will lead statistical analysis for clinical studies, develop analysis databases, and liaise with cross-functional teams. Responsibilities include statistical programming, data review, and oversight of CRO services.

The Project Coordinator will support the development of RNAi therapeutics, monitoring timelines, facilitating communication across teams, and managing program plans.