studies and regulatory submissions. Key Responsibilities: Analysis and reporting of clinical trial data using SAS and/or R... statistical programming related documents for regulatory submissions Maintain tracking and validation documentation Collaborate...
studies and regulatory submissions. Key Responsibilities: Analysis and reporting of clinical trial data using SAS and/or R... statistical programming related documents for regulatory submissions Maintain tracking and validation documentation Collaborate...
programming activities to support complex statistical data analysis of clinical studies and regulatory submissions. Key... and efficacy Prepare statistical programming specifications Prepare statistical programming related documents for regulatory...
all statistical programming activities within a study. You may also support regulatory submissions. Key Responsibilities: Lead... collection to analysis reporting Proven record of superior statistical programming and problem-solving skills within clinical...