Top Biotech Jobs in Los Angeles, CA

The Associate Director, Biostatistics role involves providing statistical expertise for clinical study design and data analysis, ensuring compliance with regulations, and contributing to publications and regulatory submissions.

The Manager, Biostatistics will design clinical studies, analyze data, provide statistical input, and contribute to publications, ensuring high-quality deliverables in compliance with regulations.

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.

The GRAIL Galleri Consultant will develop sales strategies, nurture relationships with healthcare providers, and execute promotional activities to increase adoption of MCED technology in targeted regions.

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 Medical Science Liaison will support Tempus by educating healthcare professionals on oncology products and gathering insights for future developments, focusing on molecular oncology and genomic profiling.

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

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.

Negotiate, draft, review, and finalize clinical trial agreements, amendments, and ancillary documents with study sites. Maintain stakeholder communication, track contract progress in ICON/client systems, identify risks, support site start-up, file contractual documents, and participate in study team calls while adhering to SOPs and training requirements.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

The Senior CRA will monitor clinical trial sites for compliance, conduct site visits, train site staff, and manage relationships with stakeholders in ophthalmology.

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.

The Senior Associate, Document Control is responsible for managing electronic and physical record documentation, ensuring compliance, and providing training support in a biopharmaceutical environment.

The Clinical Account Manager will manage territory accounts, build relationships with healthcare professionals, analyze business performance, and educate customers about products in the rare disease and oncology sectors.

The Senior Director of Quality Assurance GCP leads compliance oversight for clinical projects, manages audits, inspections, and quality assurance functions, ensuring regulatory adherence and team development.