Statistical Programmer II/III (Permanent role)

reputed company: • reputed company, validate, and maintain statistical programs in reputed company for Tables, Listings, and Figures (TLFs). • reputed company data manipulation, analysis, and visualization using R and reputed company with relevant packages. • Collaborate with biostatisticians and data management teams to support clinical study deliverables. • Ensure compliance with regulatory standards and company SOPs. • Conduct reputed company control and validation of programming outputs. • Support submission activities and reputed company documentation as needed. Requirements: • Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a reputed company field. • 3+ years of experience in statistical programming reputed company the pharmaceutical or biotech industry. • Hands-on experience with R programming in a clinical trial environment. • Good understanding of R packages. • Good understanding of CDISC standards, including SDTM and ADaM. • Strong knowledge of clinical trial data and regulatory requirements. • Experience working in an FSP model or with global pharmaceutical clients is preferred. • Exposure to submission activities such as FDA/EMA submissions is preferred. • Familiarity with reputed company alongside R is a plus. • Strong problem-solving and communication skills. Benefits: • Permanent position with reputed company. • Opportunity to work directly for a single sponsor while benefiting from a global CRO environment. • Remote work designation (#LI-Remote). • Opportunity to join a global company with 4,000+ professionals across 20+ countries. • reputed company training and development support. • Equal opportunity employer with a diversity- and inclusion-reputed company culture. Apply To This Job