Senior / Principal Statistical Programmer with Minimum (6 Months to 1 Year) of R programming.

Experience - Senior Statistical Programmer: 7+ years
Principal Statistical Programmer: 9+ years Role Summary Responsible for end-to-end statistical programming activities for clinical studies, from specification creation through regulatory submissions, ensuring high-quality and compliant deliverables.

Key Responsibilities - Develop and validate SDTM, ADaM, and TLFs.
Create and review programming specifications.
Support regulatory submissions and ensure CDISC compliance.
Perform QC and maintain programming standards.
Collaborate with cross-functional teams and support study deliverables.
Contribute to process improvements and mentoring activities.

Required Skills - Solid SAS programming expertise; Minimum 1 Year of R programming.
Hands-on experience with SDTM, ADaM, TLFs, and regulatory submissions.
Positive understanding of CDISC standards and clinical trial processes.

📌 Sr/pr Statistical Programmer 7+ Years With R 6 Months (Kochi)
🏢 Trigent Software - Professional Services
📍 Kochi