India onlyAs a Principal Statistical Programmer, you will work on clinical development programs, oversee CRO programmers, and deliver high-quality statistical programming results. You will be responsible for implementing reporting and analysis activities for Sponsor clinical trials, including generating datasets, listings, tables, and graphs.
Requirements
- Strong programming skills in SAS and/or R
- Experience with SDTM and ADaM specifications
- Knowledge of FDA regulations and good clinical practice
- Excellent analytical and problem-solving skills
- Ability to work independently with minimal supervision
- Strong collaboration and communication skills
Benefits
- Competitive salary and benefits package
- Opportunity to work with a global pharmaceutical client
- Collaborative and innovative work environment
- Professional development and growth opportunities
United States
Canada only
FR, IT + 3 more
