Statistical Programming Contractor (SAS, CDISC, Hybrid)

Crispr-Therapeutics-1; Boston (MA); Hybrid; USD 96,000 - 110,000; Full time

Benefits offered by this job

On-site 3 days/week

Remote work flexibility

Competitive hourly pay

Job summary

CRISPR Therapeutics is seeking a Statistical Programming Contractor to support SAS programming for clinical studies and FDA submissions. You will design, validate, and modify SAS programs, create CDISC datasets, and produce high-quality tables, figures and listings.

Responsibilities include collaboration with Clinical Operations, Data Management and Biostatisticians to ensure timely data analysis. A Bachelor’s in Statistics/Math/CS is required, with a Master’s preferred and 3+ years in

Qualifications

• Bachelor’s degree in Statistics, Mathematics, and/or Computer Science; Master’s degree preferred.
• Minimum 3 years of statistical programming in a pharmaceutical/biotech or CRO setting, depending on level.
• Strong knowledge of CDISC including SDTM and ADaM, metadata, terminologies, and FDA data submission readiness.
• Advanced SAS programming skills for SDTM, ADaM, Tables, Figures and Listings; experience with SAS/BASE, SAS/STAT, SAS/GRAPH and Macro language.
• Good understanding of GCP/ICH 21 CFR Part 11.

Responsibilities

• Design, develop, evaluate, validate and modify SAS programs for clinical data analysis.
• Create and validate CDISC standard datasets and related tables, figures and listings.
• Produce quality edit checks and efficient reports within timelines.
• Collaborate with Clinical Operations, Data Management and Biostatistics to support data analysis.

Education

Bachelor's degree in Statistics, Mathematics, and/or Computer Science

Master’s degree preferred

Tools

SAS/Base

SAS/STAT

SAS/GRAPH

SAS Macro language

CDISC SDTM/ADaM

Job description

CRISPR Therapeutics is seeking a Statistical Programming Contractor to support SAS programming for clinical studies and FDA submissions. You will design, validate, and modify SAS programs, create CDISC datasets, and produce high-quality tables, figures and listings.

Responsibilities include collaboration with Clinical Operations, Data Management and Biostatisticians to ensure timely data analysis. A Bachelor’s in Statistics/Math/CS is required, with a Master’s preferred and 3+ years in