Top Biotech Jobs in Los Angeles, CA

Responsible for scientific oversight and quality of late-stage oncology clinical trials, partnering with colleagues to ensure successful execution, protocol authoring, and data analysis.

The Manager, RPMSS oversees regulatory program management for Pfizer Oncology, ensuring strategic alignment and timely submissions while enhancing workflow efficiency and supporting cross-functional teams.

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 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.

The Sales Director will lead the sales process to close partnerships with research sites, managing all sales activities including discovery and negotiation, while collaborating with Customer Success for onboarding.

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

The role involves supporting commercial objectives by educating healthcare providers on Tempus oncology products through presentations and managing key relationships in oncology.

As an Account Services Representative, you'll provide customer support through phone and email, manage inquiries, and ensure quality order processing. You'll also adapt to rapid changes and participate in improvement projects.

The Product Manager will lead the laboratory-scale filtration product portfolio, focusing on innovation, development, market strategy, and revenue growth, ensuring alignment with customer needs and industry trends.

The Clinical Trials Associate will support the administration of clinical trials, ensuring compliance with regulations, maintaining documentation, and facilitating communication between clinical sites and the operations team.

The Clinical Document Management Specialist supports clinical trials by managing essential study documents, ensuring compliance with SOPs and regulatory guidelines.

The Manager will oversee Capex projects in GMP environments, ensuring compliance with regulations, managing contractors, and leading engineering initiatives for manufacturing operations.

The Project Director will lead large, complex facility and equipment improvement projects, ensuring adherence to safety, fiscal control, and project execution from concept to completion.

The Business Engagement Manager connects Genentech with healthcare financial decision-makers, manages provider contracts, ensures compliance, and drives patient access within the ecosystem.