Contract Statistical Programmer - CDISC/SDTM, SAS

CRISPR Therapeutics; Boston (MA); On-site; USD 96,000 - 110,000; Full time

Job summary

CRISPR Therapeutics seeks a Statistical Programming Contractor to support statistical programming activities for assigned clinical studies, FDA submissions, and related initiatives.

You will design, develop, validate and modify SAS programs to analyze data, create CDISC standard datasets, and produce quality tables, figures and listings through collaboration with Clinical Operations and Biostatistics.

Qualifications

• Bachelor’s Degree in Statistics, Mathematics, and/or Computer Science/IT background (Master’s preferred).
• Minimum 3 years of statistical programming experience in pharma/biotech/CRO.
• Strong knowledge of CDISC SDTM/ADaM, metadata, terminologies and FDA data submission processes.
• Proficient SAS/BASE, SAS/STAT, SAS/GRAPH and SAS Macro language.

Responsibilities

• Design, develop, evaluate, validate and modify SAS programs for clinical data analysis.
• Create and validate CDISC standard datasets.
• Program edit checks and produce quality tables, figures, and listings in a timely manner.
• Collaborate with Clinical Operations, Data Management and Biostatistics on projects to enable timely data analysis.

Skills

Statistical programming

CDISC knowledge

SAS programming

GCP/ICH knowledge

Education

Bachelor’s Degree in Statistics, Mathematics, or Computer Science/IT

Master’s Degree preferred

Tools

SAS

Job description

CRISPR Therapeutics seeks a Statistical Programming Contractor to support statistical programming activities for assigned clinical studies, FDA submissions, and related initiatives.

You will design, develop, validate and modify SAS programs to analyze data, create CDISC standard datasets, and produce quality tables, figures and listings through collaboration with Clinical Operations and Biostatistics.