Top Biotech Jobs in Los Angeles, CA

The Director, Medical Insights will advance Pfizer's Medical Insights capabilities, focusing on strategy, insight generation, and maximizing impact through analytics and AI while collaborating with key stakeholders.

Lead the Oncology scientific communications strategy and execution ensuring alignment with TA priorities, engaging stakeholders, and managing budgets and deliverables.

The Director, Clinical Development Scientist is responsible for leading clinical trials' scientific integrity, protocol development, compliance, and risk management, ensuring timely execution and effective collaboration with stakeholders.

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.

The Senior CRA manages clinical trial activities, ensures compliance with protocols and regulations, and supports site staff to maintain trial integrity.

The Senior CRA oversees clinical trial activities, ensuring compliance with protocols and regulatory standards, managing multiple sites, and providing training. Strong organizational and interpersonal skills are crucial.

The Clinical Research Associate will monitor oncology clinical trials, ensure compliance with regulations, support site training, and maintain documentation.

The RBM will lead sales initiatives and account management for Negative Pressure technologies, collaborate with cross-functional teams, and achieve business goals through strategic targeting and clinical value propositions.

The Publication Specialist/Document Manager oversees publication documentation, manages iEnvision issues, assists in content creation, and coordinates meetings and compliance with MPRC governance.

The role involves providing expertise in Risk-Based Quality Management (RBQM) and central monitoring in clinical trials, ensuring compliance, risk assessment, and promoting operational excellence through data analytics and process improvement.

Manage interdisciplinary clinical research studies, ensuring compliance with regulations. Act as liaison, oversee project teams, and ensure quality, timelines, and budget management.

The Territory Manager will lead business development efforts, manage sales channels, and develop professional relationships with municipal and industrial clients to drive sales in wastewater treatment.