Statistical Programmer II

This is an opportunity for an experienced statistical programmer to join a globally recognised clinical research organisation at its Kochi, Kerala office. The role sits within a team that delivers data programming and analytical solutions across clinical development programmes.

The successful candidate will be responsible for developing, validating, and maintaining SAS programs or equivalent statistical code used in the analysis and reporting of clinical trial data. Work will span activities such as CDISC-compliant dataset creation (SDTM and ADaM), table, listing, and figure (TLF) generation, and support for regulatory submissions.

• Key responsibilities: Writing and validating SAS or equivalent programs for clinical data analysis; creating and reviewing SDTM and ADaM datasets in line with CDISC standards; generating tables, listings, and figures for clinical study reports; collaborating with biostatisticians, data managers, and project teams; contributing to submission-ready documentation.
• Required skills and experience: Proficiency in SAS programming within a clinical trials environment; working knowledge of CDISC standards (SDTM, ADaM); familiarity with regulatory submission requirements; strong attention to detail and the ability to work to tight timelines.

This position offers the chance to work on complex, multi-phase clinical studies within a structured and collaborative environment. Candidates with a background in biostatistics, life sciences, or a related field and relevant hands-on programming experience are encouraged to apply.