Senior Statistical Programmer

About the role

Be Part of One Team, One Purpose. With over 47 years of scientific excellence , we've led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience. Through our two business units— Emmes, a full-service CRO , and Veridix AI, our technology, data, and analytical solutions —we are modernizing clinical trials and accelerating the development of life-changing therapies.

What you'll do

• Develop, test, and validate SDTM and ADaM datasets according to CDISC standards
• Program Tables, Listings, and Figures (TLFs) in support of clinical study reports (CSRs) and regulatory submissions
• Translate statistical analysis plans (SAPs) into accurate and efficient code
• Serve as the lead programmer on individual studies or studies within a program
• Collaborate with cross functional teams including Biostatisticians, Clinical Data Managers, and Regulatory personnel

What you need

• 4–6 yrs of experience
• Regulatory affairs
• SAS
• CRO
• Clinical research
• Documentation
• SOP writing
• B.Tech or B.E. or B.Sc or BCA or M.Tech or MCA or M.Sc

Good to have

• SQL
• R
• Python
• GCP
• VBA