Provides medical input to Clinical Trial Protocol, Investigator's Brochure, Informed Consent Form, Independent Data Monitoring Committee Charter, Statistical Analysis Plan, Medical Monitoring Plan, Clinical Trial Report, Clinical Trial Overview Statements and other clinical trial documents * Supports data analysis and interpretation of collected data to assess the efficacy and safety of the compound/intervention, including statistical evaluation and comparison to predefined endpoints * Interprets clinical trial medical data for Clinical Trial Reports and submission documents
mehr