Hiring: Associate Director/Director Biostatistics Company: Verastem Oncology Location: Massachusetts, United States Job Posted Time: 2026-09-16 15:46:15 Target Skills & Keywords : Project Management About the job Experience: •8 years of relevant clinical trial experience, or MS in statistics or equivalent with at least 10 years of relevant clinical trial experience. •At least 8 years of relevant clinical trial experience, or MS in statistics or equivalent with at least 10 years of relevant clinical trial experience. Required Skills: •Lead statistical work for one or two studies, support other studies as needed, and serve as the statistical point of contact. •Perform and assist with formulation of statistical analyses of clinical trial data to advance clinical development programs and facilitate external collaborations; communicate interpretation of results cross-functionally. •Execute pre-defined statistical regulatory strategy and support regulatory submissions and interactions as needed from a biostatistics and programming perspective; provide responses to regulatory requests; ensure team understanding of the statistical aspects of regulatory interactions. •Contribute to and support authoring of protocol sections on statistical methods and review or edit other sections, including endpoints, objectives, and assessments, by applying statistical principles. •Author or oversee creation of statistical analysis plans for studies and integrated summaries; author or edit shells for tables, figures, and listings. •Execute statistical aspects of data monitoring committee charters, project management plans, and other study-level documents. •Ensure the quality of assigned statistical deliverables. •Conduct statistical modeling to enable rigorous and efficient study designs and address identified or potential statistical issues arising in studies or programs. Qualifications: •PhD in statistics or a related field with at least 8 years of relevant clinical trial experience, or MS in statistics or equivalent with at least 10 years of relevant clinical trial experience. •Strong communication skills and ability to work effectively with cross-functional teams. •Knowledge of statistical methods for clinical trials. In-depth knowledge of FDA, EMA, and ICH regulations and guidelines. Experience with NDAs, MAAs, and other regulatory submissions is preferred. Proficiency in statistical programming; SAS is required and R is preferred. Experience with clinical trial design. •Strong organizational, analytical, and problem-solving skills; ability to manage changing priorities in a fast-paced environment; and a positive, collaborative approach. •Oncology clinical trial experience preferred. Compensation: •$200,000 - $265,000 / 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!