Senior Manager, SAS Macro Developer

About the role

Global Clinical Development team at Sun Pharma drives enterprise-level SAS macro solutions for clinical trial reporting. The Senior Manager leads design, development, and validation of reusable SAS macros for TLF, SDTM, and ADaM workflows, mentors junior programmers, and partners with biostatisticians to ensure GxP compliance. Hybrid role based in Gurgaon, India with remote flexibility, offering leadership in automation strategy and regulatory submission support.

What you’ll do

• Design and implement complex, reusable SAS macros for TLF generation
• Develop automated tools for data transformation and quality control
• Ensure macro development adheres to SDLC and 21 CFR Part 11 compliance
• Validate and document macro performance and functionality
• Collaborate with statistical programmers and biostatisticians to translate requirements
• Mentor junior staff and lead training initiatives
• Optimize macro performance for large clinical datasets
• Provide expert support for macro integration during study submissions

What you’ll bring

• 12+ years SAS programming in pharma/biotech
• 5+ years dedicated SAS macro development
• Experience with Pinnacle 21 CDISC validation
• Familiarity with R, Shiny, or Python
• Strong SDLC and GxP compliance background
• Deep knowledge of CDISC standards (SDTM, ADaM, Define-XML)
• Excellent communication and global team collaboration
• Mentoring and training junior developers

Skills

Education

Master's or Bachelor's in Computer Science, Statistics, Mathematics, Life Sciences or related field