Job Responsibilities:
• Assists in writing statistical analysis plans and system programming plans for all phases of clinical studies.
• Supports the basic activities of clinical study design related to the implementation of a clinic.
• Coordinates training schedules and presentation materials for the training of statisticians and non-statisticians on statistical methods and tests.
• Formats reports on the findings of statistical analyses and publications in preparation for new product applications to regulatory agencies.
• Assists senior staff with the preparation and documentation of facts to write and support trial reports and publications
• Supports the implementation of new and revised statistical standards, tests, and processes for increased accuracy and efficiency.
• Coordinates documents and findings of revised changes to submission to management.
• Maintains important information on data management, investigator initiated trials, and registries.
• Routes questions to senior biostatistics staff on statistical issues from the business units and external customers