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Hiring: Statistical Programmer – Clinical Data (SAS/R)Locations: Mumbai | Pune | Bangalore | Hyderabad | DelhiIndustry: Pharma / Biotech / Clinical Research⏳ Experience: 3–12 YearsAbout the RoleLatinum HR is hiring a Statistical Programmer – Clinical Data for a leading Pharma/Biotech organization. This role plays a key part in supporting clinical trials, regulatory submissions, and integrated analyses while ensuring high-quality statistical programming deliverables across the drug development lifecycle.Key Responsibilities- Lead statistical programming activities for assigned compounds or therapeutic areas - Create and validate ADaM datasets, TFLs in compliance with CDISC standards - Develop and validate ISS and ISE for regulatory submissions - Build, test, and maintain reusable SAS programs and macros - Prepare reviewer guides, define.xml, and regulatory documentation - Mentor and guide junior statistical programmers - Collaborate closely with Biostatistics, CDM, Clinical, and Regulatory teamsRequired Skills & Experience- Strong hands-on experience in SAS programming (R experience is a plus) - In-depth knowledge of CDISC standards (ADaM, SDTM) - Experience supporting FDA / EMA regulatory submissions - Understanding of clinical trial processes and data flow - Exposure to therapeutic areas such as Oncology, Immunology, or Neuroscience - Strong communication and leadership capabilitiesWhy Join Us?- Work on global, cutting-edge clinical trials - Be part of a high-impact data-driven environment - Collaborate with experienced professionals in life sciencesInterested candidates can share their CVs at:samiksha@