Top Biotech Jobs in Los Angeles, CA

Provide scientific oversight and data quality for late-stage oncology clinical trials; author protocols and regulatory documents; analyze emerging safety and efficacy data; partner cross-functionally to execute phase 3/pivotal programs and support regulatory submissions and governance.

The Associate Director, Biostatistics is responsible for statistical guidance in clinical study design, data analysis, and regulatory submissions, leading clinical study teams to ensure timely and quality outcomes.

Lead clinical execution and oversight of medium-to-high complexity trials, ensuring participant safety, regulatory compliance, and data integrity. Develop and author protocols, informed consent, safety plans, and clinical reports; manage risk, committees (DMCs), and external investigators. Provide strategic clinical input across study design, SAP/BDR, site selection/training, and audit/inspection responses.

The Payer Engagement Account Director will drive payer opportunities, build relationships with payers, lead meetings, and collaborate cross-functionally to advance access to the company's cancer detection technology.

As a Senior Data Engineer, you will design and develop AI-powered data solutions, investigate tools, and collaborate with engineering to enhance Sleuth's platform.

The Chief Operating Officer will lead operational execution and manage delivery teams, drive company-wide operating rhythms, and partner closely with the CEO and leadership team to scale the organization and enhance operational effectiveness.

The Key Account Director, Data & AI Apps will expand client relationships with pharmaceutical companies, driving revenue through the use of Tempus' platform in precision medicine. Responsibilities include developing account strategy, maintaining executive relationships, negotiating contracts, and collaborating with cross-functional teams to deliver value.

The Senior Payroll Specialist oversees US payroll processing, supports EMEA payroll, ensures compliance, and drives cross-functional process improvement initiatives.

As a Senior CRA, you will oversee clinical trial activities, ensuring compliance with protocols, conducting site visits, and training site staff.

The Clinical Site Associate supports clinical trial operations by managing site communications, maintaining documentation, and ensuring compliance. Requires collaboration with Clinical Research Associates and cross-functional teams.

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

The Immunization Specialist increases vaccine uptake among healthcare providers through education and engagement, supports inventory management, and collaborates with cross-functional teams to overcome barriers and enhance compliance.

Manage biomarker studies and oversee biomarker operations in clinical trials, ensuring high standards in sample collection and analysis. Lead cross-functional teams through the trial lifecycle while managing project timelines, budgets, and quality.

The Principal Biostatistician leads RWD studies, mentoring biostatisticians, preparing statistical plans, reviewing data, and ensuring high-quality project completion. Requires RWD experience and a PhD.

The Technical Development Manager oversees growth of the product pipeline, fosters supplier relations, conducts technical training, and supports sales with market insights and promotional activities.