Job Description : Senior Statistical Programmer
Company Description :
Element Technologies is an AI and digital transformation company focused on delivering measurable outcomes. We empower enterprises to move beyond traditional automation into a smarter, adaptive future with advanced technologies such as Agentic AI, Generative AI, and Intelligent Document Processing (IDP). Serving industries like Life Sciences, Financial Services, Retail, Media, and Tech, we specialize in enterprise-grade AI platforms, scalable digital ecosystems, cloud-native architecture, and innovative solutions. Our purpose-driven approach and passion for technology help businesses accelerate their digital transformation journey.
Role Description :
We are seeking a Senior Statistical Programmer with 3-6 years of experience to join our team in India. This is a full-time, on-site role responsible for designing, developing, validating, and maintaining statistical programs for clinical trials. The role requires close collaboration with biostatisticians, data managers, and cross-functional teams to ensure data accuracy, compliance with standards, and timely delivery of outputs.
Key Responsibilities (KRA) :
- Develop, validate, and maintain statistical programs to generate analysis datasets, tables, listings, and figures (TLFs).
- Ensure compliance with CDISC standards including SDTM and ADaM.
- Collaborate with biostatisticians, data managers, and clinical teams to ensure high-quality deliverables.
- Perform validation and quality checks to ensure accuracy, consistency, and integrity of clinical trial data.
- Prepare and document programming specifications, processes, and outputs.
- Contribute to the development and implementation of programming standards, procedures, and best practices.
- Support regulatory submissions by preparing compliant datasets and outputs.
- Troubleshoot and resolve programming issues efficiently.
- Provide mentorship and technical guidance to junior programmers when required.
Required Skillsets :
3-6 years of experience in statistical programming for clinical trials.Proficiency in SAS with exposure to R (upskilling to proficient encouraged).Strong knowledge of CDISC standards (SDTM, ADaM, TLF).Solid understanding of programming logic, data structures, and statistical concepts.Experience with clinical trial data analysis and reporting.Strong analytical, problem-solving, and debugging skills.Excellent attention to detail and ability to maintain data accuracy.Effective communication and collaboration skills with cross-functional teams.Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, or a related field.(ref : iimjobs.com)