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Verastem Oncology seeks an Associate Director of Biostatistics to lead statistical activities for oncology trials and oversee analysis planning, execution, and cross-functional collaboration across global teams.
The role requires a PhD in statistics (or related field) with 8+ years of trial experience, or an MS with 10+ years. SAS is essential; R is preferred to enrich analyses.
Responsibilities: perform statistical analyses, develop and review analysis plans, support regulatory submissions, author statistical sections for protocols and reports, collaborate with CROs, and communicate results cross-functionally.
Qualifications: PhD in statistics or related field with 8+ years of clinical trial experience (or MS with 10+ years), proficiency in SAS (and R preferred), strong understanding of regulatory guidelines (FDA, EMA, ICH), and experience in oncology clinical trials.
HighValue: oncology, clinical trial design, regulatory interactions, data analysis, and cross-functional collaboration.
WorkSetup: location details not specified, but requires effective communication with global teams.