Biostatistician; Senior Statistical Associate; Clinical Research

Westat is a leader in research, data collection and analysis, technical assistance, evaluation, and communications. Our evidence-based findings help clients in government and the private sector accelerate advancements in health, education, transportation, and social and economic policy. Our dedication to improving lives through research and our approach to projects grounded in investigative curiosity, statistical and data rigor, adaptive methods, and advanced technology are why clients find exceptional value in our work.

Westat is a leader in research, data collection and analysis, technical assistance, evaluation, and communications. Our evidence-based findings help clients in government and the private sector accelerate advancements in health, education, transportation, and social and economic policy. Our dedication to improving lives through research and our approach to projects grounded in investigative curiosity, statistical and data rigor, adaptive methods, and advanced technology are why clients find exceptional value in our work.
Westat is seeking a Senior Statistical Associate - Biostatistician to support statistical analyses on various clinical research projects involving data from clinical trials, clinical and epidemiologic studies, and administrative datasets. In this role, you will collaborate with sponsors, external investigators, and internal project team members on a variety of federal research projects, including Phase 1- 4 randomized clinical trials. You will contribute to the design of cutting-edge studies, conduct data analysis for Westat projects, and contribute to peer-reviewed scientific publications.

You will present computational and statistical analysis results to collaborators and assist them with data access, analysis, and interpretation of results. You will build appropriate algorithms and techniques to answer defined clinical and treatment outcomes and epidemiologic questions, ensuring that results are scientifically robust and well documented.
This role requires working onsite at our office in Bethesda, Maryland office 2 days per week and 3 days per week from your home office.

• Collaborate with sponsors, external investigators and other Westat staff on the development and review of study protocols, including the selection of appropriate trial/study designs and statistical methodology with special emphasis on Bayesian methods.
• Develop study aims and research hypotheses and assess appropriateness and feasibility.
• Estimate optimal sample size for the desired power, recognizing resource limitations of individual research studies.
• Develop statistical considerations and analysis methods for study protocols.
• Develop statistical analysis plans for research projects including guiding the data management team in terms of database design, selection of statistical methods, creation of project timelines, and development of formats for presenting results.
• Participate in all phases of analytical programming, data management, macros, quality control and reporting of research data.
• Conduct statistical analysis for clinical trials, clinical studies and epidemiological projects including implementation and refinement of statistical methods, preparation of formatted tables of results and other outputs, verification of the accuracy of results, and assumption of primary responsibility for the analysis and presentation of project data.
• Contribute to efforts in researching, recommending, and implementing methods to validate, troubleshoot, and interpret results.
• Participate in quality control and quality assurance processes and review code output, tables, and charts.
• Present analytic results orally and in writing to internal and external audiences, incorporating descriptions of methods, relevant literature, and other background material to provide context for the results.
• Serve as a data resource for research project teams and interact directly with clients and external investigators.

• PhD in Biostatistics or a related quantitative field of study and 2-4 years of post-doctoral relevant experience, including 1-2 years in the design, analysis, interpretation, and reporting of clinical trials.
• Experience in health research, advanced data analysis, and in analyzing research data using statistical packages.
• Experience with R, SAS, and other statistical packages.

• Skill and expertise in a broad range of statistical methods and approaches for clinical…