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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 therapies, we are driven by a passion for improving patient outcomes and addressing unmet medical needs. Our dynamic team combines expertise from both large pharmaceutical companies and agile biotech startups, fostering a collaborative environment where individual contributions are valued and innovation thrives.
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 CMC sections of the regulatory submissions.  
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.   With a strong focus on translating groundbreaking research into transformative therapies, we are driven by a passion for improving patient outcomes and addressing unmet medical needs. Our dynamic team combines expertise from both large pharmaceutical companies and agile biotech startups, fostering a collaborative environment where individual contributions are valued and innovation thrives.
Category
Regulatory Affairs
ID
2024-1132