SAS Clinical, Metadata

SAS Clinical Programmer We are seeking an experienced SAS Clinical Programmer with strong expertise in Clinical SAS, Metadata Repository, and CDISC standards (SDTM/ADaM). The ideal candidate will be responsible for developing and validating clinical datasets, maintaining metadata repositories, and supporting the generation of regulatorycompliant deliverables. Key Responsibilities Develop and validate SDTM, ADaM datasets, and TLFs using SAS. Manage and maintain clinical Metadata Repository standards and documentation. Ensure compliance with CDISC standards and regulatory requirements. Review study documents such as protocols, SAPs, and CRFs to support programming activities. Perform quality checks and support submissionready deliverables. Collaborate with crossfunctional teams to ensure timely project delivery. Requirements Strong programming experience in Base SAS and Clinical SAS. Handson experience with Metadata Repository management. Indepth knowledge of CDISC standards, including SDTM and ADaM. Understanding of clinical trial processes and regulatory guidelines. Excellent analytical, problemsolving, and communication skills. Bachelor's or Master's degree in Life Sciences, Statistics, Computer Science, or a related field. Work Arrangements Fulltime position Location: Bengaluru, Karnataka, India .