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, ADa M, 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 Strong SAS programming expertise; Minimum 1 Year of R programming. Hands-on experience with SDTM, ADa M, TLFs, and regulatory submissions. Good understanding of CDISC standards and clinical trial processes.
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