Hiring: Senior Director Biostatistics Company: Verastem Oncology Location: Massachusetts, United States Job Posted Time: 2026-09-16 15:46:20 Target Skills & Keywords : Project Management About the job Experience: •13 years of relevant clinical trial experience or MS in statistics or equivalent with at least 15 years of relevant clinical trial experience •At least 13 years of relevant clinical trial experience or MS in statistics or equivalent with at least 15 years of relevant clinical trial experience Required Skills: •Serve as a biostatistics leader within the organization, and manage statistical efforts for multiple clinical studies across a clinical program; provide leadership and guidance to other members of biostatistics and statistical programming team •Formulate, carry out, and oversee statistical analyses of clinical trial data to advance clinical development programs and to facilitate external collaborations; communicate interpretation of results cross-functionally •Lead regulatory submissions as needed including from a biostatistics and programming activities perspective; provide response to regulatory requests independently; ensure applicable understanding of team members of statistical aspects of regulatory interactions •Author protocol sections on statistical methods and review/edit other sections including (but not limited to) endpoints, objectives and assessments, by applying statistical principles •Author or oversee creation of statistical analysis plans for studies and/or ISS/ISEs; author/edit shells for tables, figures and listings •Provide statistical input to independent data monitoring committee (IDMC) and independent review committee (IRC) charters, project management plan, and other study-level documents •Create and manage timelines for SAPs, analysis specifications, and IDMC documents as needed by project/study teams •Conduct statistical modeling to enable robust and efficient statistical designs and to address identified or potential statistical issues arising in studies or programs Qualifications: •PhD in statistics or a related field with at least 13 years of relevant clinical trial experience or MS in statistics or equivalent with at least 15 years of relevant clinical trial experience •Knowledge of statistical methods for clinical trials •In-depth Knowledge of FDA, EMA and ICH regulations and guidelines •Proficient in statistical programming (SAS is required and R is a plus) •Good communication skills and ability to work with cross-functional study teams •Good organizational skills, sufficient to multi-task in an extremely fast-paced environment with changing priorities •Good analytical and problem solving skills •Oncology clinical trial experience preferred Compensation: •$265,000 - $310,000 / year •Competitive benefits and rewards package Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!