Associate Director, Biostatistics

Role: Statistical Scientist supporting hematology clinical studies, focusing on data analysis, protocol development, and regulatory submissions. Responsibilities: develop study protocols and SAPs, collaborate on database design, ensure analysis compliance, interpret clinical trial data, and prepare reports for internal teams and health authorities. Qualifications: PhD in Statistics or related field with 5+ years, or Master's with 8+ years in clinical drug development; proficient in SAS or R; experience with clinical trials and regulatory guidance; oncology experience preferred. HighValue: hematology, clinical trials, data analysis, regulatory submissions, potential involvement in manuscript/presentation development. WorkSetup: no travel required.