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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, as well as administrative support relating to the company’s contracts and other legal matters.  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
We are seeking a highly motivated and highly collaborative Research Associate/Senior Research Associate to join the Analytical Development (AD) team in implementing cell-based assays to characterize Nkarta’s pipeline of cellular immunotherapy products.
Category
Analytical Development
ID
2024-1135
Job Locations US-CA-South San Francisco
We are seeking a highly motivated Clinical Scientist to join our Cell Therapy Program for Autoimmune Diseases within our clinical development team. The ideal candidate will have a solid background in clinical research, with experience in both large pharmaceutical and small biotech settings. This role offers the opportunity to work on cutting-edge projects in a fast-paced environment, driving the advancement of novel cell therapies from early development through to clinical trials.   With a strong focus on translating groundbreaking research into transformative...
Category
Clinical Operations
ID
2024-1134
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
Job Locations US-CA-South San Francisco
The Associate Director/Director, GCP Quality Assurance oversees GCP activities at Nkarta, our CROs and Investigator Sites, leads GCP audits and inspection readiness. The successful hire will ensure high quality execution of clinical trials from first in human through commercial marketing authorization by Health Authorities for of our cellular therapy drug candidates, which are predominantly CAR-NK cell-based. This person will manage cross functional relationships with internal and external stakeholders and be the Lead Clinical Quality Assurance representative to clinical teams.  
Category
Regulatory Affairs
ID
2024-1132