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The Clinical Data Manager will oversee clinical trial data management activities, ensuring data accuracy, integrity, and compliance with regulatory standards while coordinating with cross-functional teams.

The Senior Statistical Programmer Consultant will manage programming tasks for clinical trials, oversee deliverables, and validate datasets while ensuring compliance with industry standards.

The Senior Statistical Programmer Consultant supports clinical programming tasks, ensuring high quality deliverables, compliance with standards, and collaboration with the study team. Requires expertise in oncology and statistical programming.

Lead statistical activities for oncology clinical trials, providing strategic input, developing analysis plans, and mentoring junior statisticians. Collaborate on regulatory submissions and ensure compliance with standards.

The Clinical Supply Specialist manages clinical supply execution including planning, shipment oversight, inventory tracking, and coordination with stakeholders and vendors across EU and US.

Lead cross-functional teams to manage complex clinical trials across various health sectors while ensuring compliance with GCP and regulatory standards.

Lead and manage clinical projects, ensuring compliance with regulations and overseeing trial operations, specifically in hematology and oncology.

The Principal Statistical Programmer Consultant leads programming efforts for clinical studies, ensuring quality deliverables and compliance with industry standards, while collaborating with study teams and managing concurrent project activities.

The Principal Data Scientist Consultant will develop and maintain clinical datasets using R, ensure CDISC compliance, generate reports, and contribute to internal tools while collaborating with clinical teams.

The Senior Biostatistician will lead statistical strategy for clinical trials, oversee deliverables, ensure regulatory compliance, and support cross-functional teams.