Lyell Immunopharma is a clinical-stage biotech company advancing next-generation CAR T-cell therapies for solid tumors and hematologic malignancies. Our product candidates leverage novel technology to enhance T-cell durability and efficacy, aiming for consistent long-lasting clinical responses. Founded by cell therapy pioneers, Lyell operates as a fully integrated entity from discovery to clinical evaluation, driven by values of Science, Respect, Collaboration, and Courage.
Open Positions
Director, Clinical Operations
17 years experience, MSc, 8 years in Oncology drug development, 3 years in early-stage drug programs
Associate Director, Biostatistics
PhD in Statistics, Biostatistics, Mathematics, or related fields with a minimum of 8 years' experience and a strong leadership track record in clinical development
Program Manager II - Contract role
BA/BSc in a life science discipline or related field with 10 years' biotech experience, or MA/MSc with 7 years' biotech experience. 3 years' cross-functional clinical development program management experience, preferably with late stage clinical development
Vice President, Clinical Development
MD or MD/PhD required, 12+ years of pharmaceutical/biotech industry experience, 8+ years of clinical research experience in oncology
Sr. Specialist, Electronic Quality Management Systems (eQMS)
10+ years of experience in biopharmaceutical or life sciences environments, with demonstrated technical depth in regulated GMP systems
Manager, Supplier and Vendor Audit Program
10+ years of experience, BA/BSc or MBA/MSc, Professional Auditor Certification, 12 years' experience in GMP biopharmaceutical operations, 8 years' experience in GMP Quality, and 5 years' experience as an auditor
Manager, Quality Control
10+ years of experience in a GMP-regulated pharmaceutical, biotech, or related industry, with prior experience in cell therapy environments
Director, MSAT
BA/BSc in related field, 15+ years experience in GMP biopharma (or 10+ with 5+ in MS level), and an MBA/MSc. 5+ years experience in manufacturing automation & MES systems
Senior Associate, Quality Assurance
BS degree, 7+ years experience, proficiency in GMP Platforms, and familiarity with Cellular and Lentiviral Vector manufacturing
Director, Field Medical
PharmD, PhD, MD, or DO with 5+ years experience in a field medical or MSL role, oncology/hematology specialty required