Experience – 5+ years Roles and Responsibilities: 1. Primarily responsible for the quality and timely delivery of SDTM artifacts (SDTM Specifications, datasets, define.xml, SDRG, Annotated CRF) 2. Programming and validation of SDTM datasets, including Trial design datasets and Efficacy domains. 3. Thorough understanding of End- the to-End SDTM process (CRF annotation- Define.xml) 4. Review the Study EDC specification and ensure all collected study data (including external) is mapped appropriately in the target SDTM model 5. Annotate CRFs for data mapping of existing raw clinical data to CDISC (version 3.1.2, 3.2) compliant SDTM datasets 6. Experience in creating SDTM mapping specification 7. Utilize Pinnacle 21 for verifying compliance of datasets with CDISC standards 8. Experience in debugging system-level SDTM macros and modifying them for study level 9. Develop utility macros for reusability and efficiency 10. Coordinate work on multiple projects according to priorities 11. Communicate effectively with the project team/stakeholders/ other departments and/or groups. ADD ON’S 1. Programming and Validation of ADAM and TLF datasets. Desired Candidate Profile Relevant experience in clinical SAS Programming of at least 6 years. Perks and Benefits Permanent work from Home Opportunity Permanent Employment with Fixed CTC and other allowances. PF, Gratuity, Mediclaim, and other reimbursements. Job Types: Regular / Permanent, Full-time Pay: ₹1,000,000.00 - ₹2,500,000.00 per year Benefits: Cell phone reimbursement Flexible schedule Health insurance Internet reimbursement Leave encashment Life insurance Paid sick time Paid time off Provident Fund Work from home Schedule: Fixed shift Flexible shift Monday to Friday Weekend availability Supplemental Pay: Joining bonus Yearly bonus