Kyverna Therapeutics

HQ
Emeryville
55 Total Employees
Year Founded: 2018

Similar Companies Hiring

Healthtech • Biotech • App development
4 Offices
70 Employees
Artificial Intelligence • Big Data • Healthtech • Software • Biotech
3 Offices
450 Employees
Cloud • Healthtech • Social Impact • Software • Biotech
4 Offices
605 Employees

Jobs at Kyverna Therapeutics

Let Your Resume Do The Work
Upload your resume to be matched with jobs you're a great fit for.

Biotech
The Paralegal will manage legal and contract administration, ensuring accuracy and efficiency in contract execution and documentation. Responsibilities include overseeing contract tracking, providing support to stakeholders, and optimizing workflow processes while maintaining high detail standards.
Biotech
The Associate Director of Clinical Data Management oversees data management activities for clinical studies, ensuring regulatory compliance and data accuracy from start-up to database lock.
Biotech
The Executive Director, Regulatory Affairs will lead regulatory strategy for cell therapies, overseeing submissions, health authority engagement, and team development, ensuring commercial readiness and compliance.
Biotech
The Executive Director, Clinical Data Management leads the data management strategy, ensuring quality clinical data and compliance throughout the clinical development lifecycle.
Biotech
The Senior Clinical Research Scientist will design, execute, and analyze clinical studies, ensuring compliance with GCP and regulatory requirements, and collaborate across multiple departments.
Biotech
The Executive Director will optimize and manage Kyverna's supply chain function, oversee supplier selection, negotiate contracts, and lead strategic sourcing efforts across multiple regions to support business growth in cell therapy.
Biotech
The Sr. Director of Business Development will drive Kyverna's growth strategy through strategic partnerships, licensing, and collaboration in the biopharmaceutical sector.
Biotech
The Publications & Conferences Manager will oversee project management of publication deliverables and support global publication strategies and conference planning activities.
Biotech
Responsible for drafting, negotiating, and managing contracts related to clinical development in a biopharmaceutical company, ensuring alignment with company policy and regulatory frameworks.
Biotech
The role focuses on evaluating and advising on CAR T technologies and immune cell engineering for autoimmune diseases, conducting scientific assessments, and liaising with internal and external stakeholders.