Strong knowledge of clinical trial data management principles, practices, and regulatory requirements. Proficiency in using clinical data management systems and electronic data capture (EDC) tools. Solid understanding of database design, data coding, and data validation techniques. Excellent attention to detail and problem-solving skills, with the ability to identify and resolve data discrepancies. Strong organizational and project management skills to effectively manage multiple projects simultaneously. Proficient in using statistical software, such as SAS or R, for data analysis and reporting. Excellent communication and interpersonal skills to collaborate with cross-functional teams and external stakeholders. Familiarity with clinical data standards, such as CDISC (Clinical Data Interchange Standards Consortium), is a plus. Knowledge of regulatory requirements, including Good Clinical Practice (GCP) guidelines and Health Insurance Portability and Accountability Act (HIPAA) regulations. Strong ethical and professional conduct to ensure data privacy and confidentiality. Contact HR SHIVA - 8438813362( What'sapp)

Role & responsibilities Data Cleaning and ManipulationDevelop 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 8438813362Preferred candidate profile Bachelors or Master's degree in biostatistics, statistics, or a related fieldMinimum of 0-2 years of experience in clinical SAS programmingStrong understanding of statistical analysis methodsExperience working with clinical trial data.Excellent SAS programming skillsProficient in data manipulation techniquesStrong communication and interpersonal skillsAbility to work independently and as part of a team.Perks and benefits