Top Biotech Jobs in San Diego, CA

The Sr. Director is responsible for developing and executing scientific communication strategies in oncology, collaborating with stakeholders, leading financial management of projects, and ensuring alignment of messaging across teams.

The Field Access Lead focuses on patient access and reimbursement strategies, educating healthcare providers, resolving issues, and maintaining compliance with corporate guidelines.

Manage LiveDesign implementation projects and ensure customer success with the Schrodinger Platform by collaborating with internal teams and representing customer needs in product development.

Lead the marketing strategy for Tempus' Oncology portfolio, drive commercial growth, craft compelling narratives, and mentor a high-performing team.

The Software Engineer will enhance developer experience by creating efficient tools for production releases and streamline workflows while collaborating with various teams.

The Principle Product Designer will lead the design of user experiences and a scalable design system to enhance AgelessRx's telehealth platform, working closely with cross-functional teams to create innovative and engaging health care solutions.

The role involves creating and managing marketing materials for the commercial team, focusing on storytelling and presentation quality while developing systems for efficiency.

The Manager, Clinical Oncology Practice Optimization will enhance operational success in community oncology practices, focusing on billing, revenue optimization, and educational resources for teams.

The Research Associate II will support routine production and innovative research related to recombinant proteins and assays, collaborating across teams while ensuring data integrity and compliance with safety procedures.

The Principal Biostatistician leads statistical analysis for clinical programs, providing input on study design, data management, and regulatory compliance while mentoring junior team members.

Oversight of document control programs and systems, ensuring compliance with regulations. Manage evaluations, improvements, and audits related to QMS and document handling.

Lead safety scientific expertise for clinical and post-market pharmacovigilance activities, prepare safety reports, and conduct safety evaluations.

The Custom Product Associate II will execute flow cytometry testing, analyze data, prepare buffers, operate lab equipment, and maintain documentation in a BSL-2 laboratory.