Senior Biostatistician

Biostatistician IIISeeking an experienced Biostatistician III to support clinical development programs by analyzing ongoing clinical trial data and providing data-driven insights to study teams. This role will partner with statisticians, programmers, and cross-functional stakeholders to monitor study progress, evaluate predefined criteria, conduct exploratory analyses, and support informed decision-making throughout the clinical trial lifecycle.Key Responsibilities:Review and analyze accumulating clinical trial data to evaluate study progress and performance metrics.Conduct exploratory, interim, and monitoring analyses to identify trends, risks, and opportunities.Partner with study statisticians, programmers, and cross-functional teams to support trial oversight activities.Develop and execute statistical analysis plans for clinical research studies.Provide timely statistical insights and recommendations to support study execution and decision-making.Support statistical planning and analysis activities across clinical development programs.Coordinate with internal and external programming teams to ensure accurate and efficient data analyses.Maintain compliance with applicable regulatory and scientific standards throughout study execution.Communicate analytical findings through reports, presentations, and technical documentation.Required Qualifications:Master's degree or Doctorate in Statistics, Biostatistics, Data Science, Mathematics, Epidemiology, or a related quantitative discipline.Minimum 5 years of experience in the pharmaceutical, biotechnology, or clinical research industry.Strong knowledge of statistical methodologies and clinical trial data analysis.Experience with statistical programming using R.Experience preparing analysis programs for Phase I, Phase II, and Phase III clinical trials.Strong understanding of clinical trial design and statistical applications within clinical research.Ability to analyze complex datasets and translate findings into actionable business and scientific insights.Excellent written, verbal, and technical communication skills.Experience conducting data monitoring, interim analyses, and exploratory analyses.Preferred Qualifications:Doctorate in a quantitative discipline.Experience using SAS for clinical data analysis.Experience serving as a lead or primary statistician for regulatory submissions.Knowledge of drug development regulations and statistical requirements supporting clinical research programs.Experience supporting New Drug Application or Biologics License Application submissions.Benefits:The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.Pay Range: $70 - $85 per hour (depending on experience)