Senior SAS Programmer Analyst – Clinical Trials

Biostatistical Consulting Inc.

Lexington (MA)

On-site

USD 90,000 - 120,000

Full time

6 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Disability insurance
FSA
401(k) with match
Annual bonus
Professional development
Private office
Onsite fitness center

Job summary

Biostatistical Consulting Inc. in Lexington, MA seeks a SAS Programmer Analyst to design and run SAS programs for clinical trial data, producing tables, listings, and figures for regulatory submissions.

This role emphasizes quality, accuracy, and working with a cross-functional team in a fast-paced setting. The candidate should have an MS/MA in statistics or biostatistics and practical SAS programming experience in clinical trials, with strong communication skills and ability to manage multiple

Qualifications

  • MS/MA in statistics or biostatistics required.
  • At least 1 year SAS programming in clinical trials for Programmer Analyst or 3+ years for Senior Programmer Analyst.
  • Excellent knowledge of SAS and ability to produce tables, listings, and figures for clinical trials.

Responsibilities

  • Develop SAS programs to analyze clinical trial data and produce tables, listings, and figures for FDA/EMA submissions.
  • Validate SAS programs and derived datasets for quality and reproducibility.
  • Prepare documentation for SAS programs.

Skills

SAS programming
Clinical trials
TablesListingsFigures
Therapeutic areas
Communication skills
Time management
Team collaboration
Meeting timelines

Education

MS/MA in statistics or biostatistics

Tools

SAS

Job description

Biostatistical Consulting Inc. in Lexington, MA seeks a SAS Programmer Analyst to design and run SAS programs for clinical trial data, producing tables, listings, and figures for regulatory submissions.

This role emphasizes quality, accuracy, and working with a cross-functional team in a fast-paced setting. The candidate should have an MS/MA in statistics or biostatistics and practical SAS programming experience in clinical trials, with strong communication skills and ability to manage multiple

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