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Job Locations US-CA-South San Francisco
We are seeking a highly motivated and collaborative QC Professional to join our team with expertise in QC and cell-based assays, critical reagents, and stability program management. The qualified candidate will coordinate closely with internal and external partners in a cross-disciplinary team of immunologists, engineers, and clinicians to develop and implement best practices in cell therapy manufacturing.
Category
Quality Control
ID
2024-1144
Job Locations US-CA-South San Francisco
The Clinical Trial Sr. Manager/Associate Director works closely with the director of clinical operations and the rest of clinical and leadership team to ensure successful execution of clinical trials. The role manages operational activities of assigned clinical programs, oversees internal and external staff for the timely and quality implementation and execution of clinical trials. Partnership with key internal and external stakeholders to ensure continuous harmonized operations of clinical operations activities is critical. Works closely with investigative site personnel, CROs, and other study vendors. Ensures conduct of clinical trial activities in accordance with Standard Operating Procedures...
Category
Clinical Development
ID
2024-1143
Job Locations US-CA-South San Francisco
We are seeking a highly motivated and collaborative Director of Viral Vector to join the Analytical Development (AD) team and lead viral vector analytical development and strategy.
Category
Analytical Development
ID
2024-1142
Job Locations US-CA-South San Francisco
Nkarta offers a unique opportunity for a highly-motivated QA Specialist to join our growing Quality Assurance team.  This role supports the qualification of our new manufacturing site and technical transfer of advanced NK cell therapies.  It’s also a key position to closely coordinate with internal and external partners in a cross-disciplinary team of immunologists, engineers, and clinicians to develop and implement best practices in cell therapy manufacturing.
Category
Quality Assurance
ID
2024-1140
Job Locations US-CA-South San Francisco
The Corporate Counsel will be responsible for managing and supporting the day-to-day contracting needs of a clinical-stage biopharmaceutical company, including drafting and negotiating a wide range of contracts and managing the contract workflow process. Although the primary focus of the role will be contracts, from time to time, the Corporate Counsel will also assist with other general corporate matters. The ideal candidate will be able to thrive in a dynamic, fast-paced environment and be a self-starter.    
Category
Legal
ID
2024-1138
Job Locations US-CA-South San Francisco
The Director, Clinical Trial Optimization leads strategic feasibility and scenario planning to inform clinical trial design that aligns the science with data driven, efficient delivery plan. This role is responsible for the review and approval of Clinical Operations strategies, SOPs and written standards, as well as a key contributor to issue review and recommendation/resolution processes. The role serves as a champion and leader for staff change management and engagement strategy, continuous improvement projects that promote individual development, team development, development of institutional knowledge, and best practices for leveraging the entire Clinical Operations network in an optimal...
Category
Clinical Development
ID
2024-1137
Job Locations US-CA-South San Francisco
We are seeking a highly organized and proactive Executive Assistant to provide comprehensive support to our Chief Financial/Business Officer and Chief Legal Officer.  The successful candidate will play a crucial role in ensuring the smooth operation of our executive offices by managing administrative tasks, coordinating schedules, organizing and tracking the status of Nkarta’s contracts, and facilitating communication within the organization.
Category
Legal
ID
2024-1136
Job Locations US-CA-South San Francisco
This role is a key critical hire for Nkarta. The role works hands-on, directly with teams and management to produce high quality clinical program documents to support regulatory submissions and scientific communications while simultaneously building up the team. For the right candidate, there is an opportunity to expand medical writing function into a central resource for the company to support both research and CMC teams in pertinent non-clinical and...
Category
Medical Writing
ID
2024-1133