SME, CDISC (Gurugram)

Sun Pharma is looking for an experienced SAS Macro Developer to join our team. The primary responsibilities of this role will be to develop and maintain SAS macros to support our SDTM (Study Data Tabulation Model), ADAM (Analysis Data Model), and TLF (Tables, Listings, and Figures) programming efforts, which are critical components of the drug development process. Key Responsibilities - Design, develop, and implement reusable SAS macros to streamline SDTM, ADAM, and TLF programming workflows - Collaborate with SAS programmers, Biostats and subject matter experts to understand business requirements and translate them into efficient macro solutions - Demonstrate a strong understanding of the drug development process and the role of SDTM, ADAM, and TLF standards in regulatory submissions - Develop macros to automate and standardize SDTM programming tasks, such as data transformation, variable derivation, and metadata generation - Maintain a good working knowledge of SDTM and ADAM standards to ensure macros are aligned with industry best practices - Optimize macro performance and ensure they are scalable and maintainable - Thoroughly test macros to validate functionality and identify/resolve any issues - Document macro code, usage, and best practices for knowledge sharing - Provide training and support to other team members on leveraging the developed macros - Stay up-to-date with the latest SAS macro language features and techniques - Will occasionally need support study team in with study SDTM/ADaM and TLFs Programming Qualifications - Education: BSc or equivalent with research experience, and/or MS (Computer Science, Bioinformatics, or Related field). Masters Degree preferred. - Minimum 7 years of experience in SAS programming, with a strong focus on macro development in Clinical development with solid knowledge of CDISC ADaM and SDTM, ICH Statistical and Clinical Report Guidelines - Experience in the pharmaceutical, healthcare, or life sciences industry is highl .