Associate Analyst, Statistical Programming
$67,000–$87,000 year
On-site · Research Triangle Park, North Carolina, United States
Job Summary
Associate Analyst, Statistical Programming supports statistical programming activities across clinical studies, including analysis datasets, tables, listings, figures, and regulatory submission deliverables. The role partners with Biostatistics and Data Management to produce high-quality, submission-ready outputs. This position contributes to study timelines, supports implementation of data standards, and assists in resolving data and programming issues under supervision. Who you are: Detail-oriented with ability to manage multiple priorities; collaborative and comfortable working cross-functionally; able to communicate progress, risks, and issues clearly. The role involves developing CDISC ADaM analysis datasets and specifications, identifying data quality issues, contributing to end-to-end programming from CRF data collection through regulatory submission, supporting preparation of submission deliverables (define.xml, XPTs, reviewer documentation), and collaborating with Biostatistics, Data Management, and Data Standards to ensure consistency and compliance. It also includes assisting with process improvement initiatives and departmental efficiency efforts.
Required Qualifications
- Bachelor’s degree in Statistics, Mathematics, or related field
- 0–2 years of SAS programming experience (Base, STAT, GRAPH, MACRO)
- Exposure to clinical trials, data management, or statistical analysis
- Basic knowledge of CDISC standards and clinical data structures
- Understanding of drug development process and regulatory requirements
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.