Fatetherapeutics
Senior Payroll Associate
Fate Therapeutics is seeking a detail-oriented Senior Payroll Associate to own our end-to-end payroll process, ensuring every employee is paid accurately and on time. The Senior Payroll Associate will manage payroll in Dayforce, including complex calculations, off cycle runs, and employee changes, w
Associate Scientist, Quality Control
Fate Therapeutics is seeking a motivated Associate Scientist to join the Quality Control (QC) team. As an individual contributor in the QC laboratory, the successful candidate will focus primarily on molecular assay execution, including digital droplet PCR (ddPCR), and DNA/RNA extraction. The Associ
Senior Director, Quality Assurance
Fate Therapeutics is looking for an experienced and hands-on Senior Director, Quality Assurance to lead our Quality organization across GxP functions. You will own the Quality Management System (QMS), ensure our clinical programs and supply chain are inspection-ready, and serve as a strategic partne
Senior Manager, Biomarker Operations
Fate Therapeutics is looking for a Senior Manager, Biomarker Operations to help advance innovative clinical programs by shaping and executing biomarker sample strategies across studies. This is an exciting opportunity for a collaborative, detail-oriented operations professional who enjoys partnering
Senior Manager, Biomarker Operations
Senior Clinical Trial Manager/Clinical Trial Manager
Fate Therapeutics is seeking a Clinical Trial Manager or Senior Clinical Trial Manager to lead complex clinical studies from start-up through close-out, ensuring high-quality execution, strong site and vendor partnerships, and timely delivery of key milestones. This role is ideal for a highly organi
Senior Clinical Trial Manager/Clinical Trial Manager
Senior Manager, Regulatory Affairs CMC
Fate Therapeutics is looking for Senior Manager, Regulatory Affairs CMC to help advance innovative cell therapy products from early development through licensure. In this role, you will shape global CMC regulatory strategy, lead high-quality submissions, partner across technical and quality teams, a
Senior Manager, Regulatory Affairs CMC
Medical Director, Autoimmunity
Provide clinical leadership of a comprehensive and integrated Clinical Development Plan for individual autoimmune programs from first-in-human studies through registrational studies. Contribute to study designs, lead protocol development, and collaborate with cross-functional teams in study start-up