Principal 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

• Lead the development, validation, and maintenance of SDTM and ADaM datasets and associated documentation
• Program complex Tables, Listings, and Figures (TLFs) for study reports, publications, and submissions
• Review and interpret statistical analysis plans (SAPs) to ensure accurate implementation in code
• Project & Study Support
• Serve as lead programmer on multiple studies and/or projects, coordinating efforts across internal teams and CROs

What you need

• 7–9 yrs of experience
• Clinical research
• SAS
• Regulatory affairs
• CRO
• SQL
• Quality control
• M.Sc or B.Tech or B.E. or B.Sc or BCA or M.Tech or MCA

Good to have

• SOP writing