Associate Director, Biostatistics

Role: Associate Director of Biostatistics supporting cross-functional development teams; contributes to trial design, analysis plans, and regulatory documentation. Responsibilities: design innovative clinical trials, defend protocols, author/review key study documents, present data analyses clearly, support health authority interactions, and ensure study consistency within therapeutic areas. Requirements: PhD (6+ years) or MS (8+ years) in statistics/biostatistics, proficiency in SAS, R, or Python, strong communication skills, and experience in clinical trials methodology relevant to drug development. Preferred: experience with regulatory processes and leading teams; prior management experience is advantageous. HighValue: supports oncology, hematology, immunology, or cardiovascular indications; involved in clinical development stages from protocol design through regulatory submission; adherence to GxP and quality standards; collaborative engagement with scientific, regulatory, and commercial stakeholders. WorkSetup: not specified.