Clinical SAS Programmer ( Looking for Bangalore and Kochi local candidates)

Role Description: This is a full-time Clinical SAS Programmer role based in Kochi with a hybrid work model, allowing a mix of on-site and work-from-home arrangements. The Clinical SAS Programmer will design, develop, and validate SAS programs to support clinical trial data analysis, reporting, and submission deliverables. Daily tasks include creating and maintaining datasets, tables, listings, and figures; performing quality checks; and ensuring compliance with regulatory and sponsor standards. The role will collaborate closely with biostatisticians, data managers, and other clinical team members to interpret study requirements and translate them into robust programming solutions. The Clinical SAS Programmer will also contribute to documentation, standardization of programming processes, and continuous improvement initiatives within the statistical programming function. Qualifications Strong expertise in Statistical Programming with 4 to 12 years of experience and in programming using SAS or similar tools, with the ability to produce high-quality, validated outputs.Solid foundation in Statistics, including understanding of clinical trial designs, analysis methods, and regulatory requirements.Experience in Data Management and handling clinical trial datasets, including data cleaning, transformation, and integration.Demonstrated Analytical Skills for interpreting study protocols, identifying data issues, and providing data-driven solutions.Bachelors or Masters degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related discipline.Exposure to CDISC standards (SDTM, ADaM) and regulatory submission requirements is highly beneficial.Ability to work effectively in cross-functional teams, manage priorities, and meet timelines in a hybrid work environment.Strong written and verbal communication skills and a detail-oriented approach to programming and documentation. .