Clinical Sas Programmer

Job Description

Role & responsibilities Data Cleaning and Manipulation Develop and execute complex SAS programs to generate analysis datasets, tables, listings, and figures according to the Statistical Analysis Plan (SAP) and study protocol. Perform statistical analyses on clinical trial data using appropriate SAS procedures, including descriptive statistics, hypothesis testing, and regression analysis. Perform statistical analyses on clinical trial data using appropriate SAS procedures, including descriptive statistics, hypothesis testing, and regression analysis. Conduct data quality checks to identify and resolve data discrepancies, ensuring data integrity throughout the analysis process. Create clear and concise clinical study reports, including tables, listings, and figures, for interim and final analysis, adhering to regulatory standards. Work closely with biostatisticians, data managers, clinical trial teams, and other stakeholders to design analyses, interpret results, and address data issues. Interested to apply can share CV or call/WhatsApp to 8438813362 Preferred candidate profile Bachelors or Master's degree in biostatistics, statistics, or a related field Minimum of 0-2 years of experience in clinical SAS programming Strong understanding of statistical analysis methods Experience working with clinical trial data. Excellent SAS programming skills Proficient in data manipulation techniques Strong communication and interpersonal skills Ability to work independently and as part of a team. Perks and benefits