@ Bangalore | Hyderabad | NCR

Office-based for the first 3 months, with the option to move to hybrid environment based on performance.

IC role, with hands-on work, 6-12yrs of experience (apply only if you have the relevant experience and expertise)

What you'll do
- Partner with statisticians to build and implement Statistical Programming Plans and SAPs, and create ADaM data specifications
- Program and validate ADaM datasets and statistical analyses in SAS/R, aligned to CDISC standards
- Generate TLFs for CSRs, safety reports, and regulatory deliverables
- Build and maintain programming documentation, macros, utilities, and QC checks
- Support audits, inspections, and regulatory submissions
- Handle cross-study and integrated analyses, plus ad hoc and exploratory requests
- Mentor and coach recent team members

What you bring
- Master's + 6 years,



or Bachelor's + 8 years, in Statistics, Computer Science, Engineering, or a related field
- Strong SAS programming (macros, data manipulation, TLF generation); R is a plus
- Advanced knowledge of CDISC standards and at least one therapeutic area - Oncology, Immunology, or Neuroscience
- Solid grounding in the drug development process and clinical study lifecycle
- Comfort with protocols, SAPs, and statistical programming documentation
- Sharp eye for detail, strong troubleshooting instincts, and clear written and verbal communication
- Ability to work with statisticians, study teams, and external partners, and adapt as priorities shift

📌 Senior Statistical Analyst (Bengaluru)
🏢 Weltrix Biometrics CRO
📍 Bengaluru