Job Description
Job Title: Statistical Programmer – Clinical Data (SAS/R)
Location : Pan India
Experience : 3 – 12 years
Industry : Pharmaceuticals / Biotechnology / Clinical Research
About the Role
We are looking for an experienced Statistical Programmer to oversee programming activities for clinical trials, regulatory submissions, and integrated analyses. This role involves leading a team, ensuring high-quality deliverables, and developing efficient programming standards to support drug development.
Key Responsibilities
- Lead statistical programming activities for a compound or therapeutic area.
- Manage, mentor, and guide a team of statistical programmers.
- Create and validate analysis data sets (ADaM), tables, listings, and figures (TFLs) following CDISC standards.
- Develop and validate Integrated Summary of Safety (ISS) and Integrated Summary...