Principal Biostatistician

Responsibilities Manage a moderate or large volume of complex tasks with minimal supervision across one or more drug programs Proactively assess and adapt solutions for the Biometrics department, resolving technical issues Make decisions at the study level across various studies, leading and prioritizing tasks globally Collaborate closely with clinical research, regulatory affairs, CROs, Commercial, Worldwide Medical, KOLs, and other disciplines Monitor needs and determine resources in consultation with line managers Participate in organization-wide initiatives such as quality and standardization efforts Requirements PhD in Biostatistics/Statistics or equivalent with 4 years relevant experience MS in Biostatistics/Statistics with 6 years relevant experience Thorough understanding of statistical principles and clinical trial methodology Ability to provide innovative and practicable technical solutions Working knowledge of medical/biological terminology and clinical trial designs Proficiency in writing and presenting information effectively Conversant with SAS programming and detailed knowledge of statistical software Working knowledge of regulatory guidelines and needs for statistical analysis Demonstrated leadership and communication skills #J-18808-Ljbffr Jobtailor