Senior Clinical Development Scientist

Role: Support late-stage oncology clinical development, collaborating with the Clinical Scientist Program Lead on trial activities including protocol design, study execution, and data analysis. Responsibilities: develop study concepts, prepare protocols and regulatory documents, contribute to data review and scientific presentations, and assist with study coordination and regulatory compliance, primarily within cancer therapies such as CAR T-cell treatments. Requirements: PharmD or PhD in clinical research/pharmacology with 6+ years' experience, or MS with 8+ years in scientific/drug development; knowledge of clinical trial design, GxP, FDA/EMA regulations, and biopharma industry standards. Preferred: experience in Multiple Myeloma or CAR T-cell therapies. HighValue: oncology, late-stage clinical trials, regulatory submissions, GxP compliance, cross-functional collaboration. WorkSetup: Not specified; travel may be required.