Statistical Analysis-Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans. -Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the analysis plan, and conducting the actual analysis once a reporting database is created. -Collaborate with data management in the planning and implementation of data quality assurance plans. -Maintain proficiency with respect to SAS programming and statistical methodology and in applying new and varied methods. -Effectively justify methods selected and implement previously outlined analysis plans. -Conduct peer-review of work products from statistical colleagues. -Effectively utilize current technologies and available tools for conducting the clinical trial analysis. -Communication of Results and Inferences -Collaborate with other statistical colleagues to write reports and communicate results. -Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers. -Assist or respond to regulatory queries working in collaboration with other statistical colleagues. Therapeutic Area and Systems Knowledge:-Understand relevant disease states in order to enhance the level of customer focus and collaboration. -Ensure replication of tools and systems, where applicable and stay informed of technological advances. Regulatory and Quality Compliance:-Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes, and training.