Senior Statistical Programmer - Clinical Data Management in Hyderabad, भारत

Job Description :- Lead clinical trial SAS programming (Phase II - IV).- Create and validate CDISC SDTM, ADaM, TLFs, and regulatory deliverables (https://jobeax.com/link/UE15fSbKOKY7scWI, eCRT).- Manage project timelines, mentor junior staff, and support multi-disciplinary clinical study https://jobeax.com/link/ZlR3JZToBtLJKlA9 Responsibilities :- Develop and validate SDTM and ADaM datasets to ensure compliance with CDISC standards and project-specific specifications for clinical study reporting.- Program complex tables, listings, and figures (TLFs) using SAS to support clinical study reports and integrated summaries of safety and efficacy.- Perform rigorous quality control and validation of programming deliverables to ensure accuracy, consistency, and adherence to regulatory guidelines.- Collaborate with cross-functional teams to resolve data discrepancies and clarify programming requirements throughout the study lifecycle.- Provide technical guidance and mentorship to junior team members to ensure project timelines and quality standards are consistently met.- Maintain comprehensive documentation for all programming activities to ensure audit readiness and compliance with internal standard operating https://jobeax.com/link/56Yblt9pfAE3JxIM :- 5 - 9 years clinical/CRO experience with 5+ years in SAS.- Expertise in end-to-end SDTMs/ADaMs, TLFs, and 2+ therapeutic areas (including oncology).- Strong background in statistics or https://jobeax.com/link/iUtActkY8Q9o1yKB Experience: 5 - 9 years (ref:hirist.tech)