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# Statistical Programming Contractor (16-Month Contract)

- **Company:** CRISPR Therapeutics
- **Location:** Boston, MA, United States (Remote available)
- **Experience:** Experienced
- **Salary:** $145,600.0 - $166,400.0
- **Contract:** Temporary contract
- **Skills:** Data Analysis, Clinical Data Repository, Computer Programming, Metadata, SAS (Software), SAS/Base, SAS/STAT, Data Streaming, Information Technology, Data Management
- **Published:** October 18, 2026
- **Apply:** https://www.disabledperson.com/jobs/76108681-statistical-programming-contractor-16-month-contract

## About the Role

* Bachelor's Degree in Statistics, Mathematics, and/or Computer Science/IT background. Master's Degree preferred.
 * Minimum 3 years of statistical programming in a pharmaceutical/biotech or CRO setting (depending on level)
 * Strong knowledge in CDISC including SDTM, ADaM, metadata, controlled terminologies, and data flows, as well as in industry standards for electronic submission of data to FDA.
 * Strong hands-on SAS programing skills and working experience for clinical trial reporting for SDTM, ADaM, Table, figure, and Listing.
 * Excellent working knowledge of SAS/BASE, SAS/STAT, SAS/GRAPH and SAS Macro language.
 * Advanced knowledge of GCP/ICH standards, 21 CFR Part 11.

Preferred Qualifications

 * Strong ability to work within cross-functional teams.
 * Excellent interpersonal, organizational, and multi-tasking skills., * Collaborative - Openness, One Team
 * Undaunted - Fearless, Can-do attitude
 * Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
 * Entrepreneurial Spirit - Proactive. Ownership mindset.

## Description

The Statistical Programming Contractor will provide technical support for statistical programming activities for assigned clinical studies, FDA submissions, and the development of initiatives.

Responsibilities

 * Design, develop, evaluate, validate and modify computer programs using SAS to analyze and evaluate clinical data.
 * Have thorough knowledge of CDISC theory and implementation guidelines, able to create and validate CDISC standard datasets
 * Program edit checks and produce quality tables, figures and listings in a timely fashion and high quality.
 * Work closely with Clinical Operations, Data Management and Biostatisticians on various clinical projects so that data analysis can be performed in a timely fashion.