Role:
Associate Director, Biostatistics at Verastem Oncology, leading statistical activities for one or two clinical studies in oncology, with a focus on cancer types driven by RAS/MAPK pathway mutations.
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.
