Biomedical Statistical Consulting is looking for an incredible SAS Programmer to join our company and support our mission of providing best-in-class statistical services to our clients and partners. We are passionate about delivering high value and assisting Sponsors' statistical needs in Regulatory Clinical Trials.

A critical step in securing FDA approval of a drug or medical device is conducting a series of clinical trials capable of demonstrating safety and effectiveness. We specialize in designing these trials, using traditional methods and innovative novel approaches such as Propensity Score Matching, adaptive clinical trial design, and Bayesian design, to save costs, work around limited access to new data, and reduce bias in non-randomized studies.

SAS Programmer job description

We are looking for a passionate and experienced SAS Programmer to join our team! SAS Programmer are responsible for transforming raw clinical trial data into analyzing datasets, providing Tables, Listings, and Figures (TLFs), and maintaining and improving analysis algorithms and processes. This job will entail close collaboration with BSC Team members, as well as Regulatory and Clinical partners. High-quality clinical trial analyses and presentation are crucial for better decision-making.

Key responsibilities

  • Process Electronic Data Capture (EDC) data into analytical datasets

  • Create Tables, Listings, and Figures to support Regulatory Clinical Trials

  • Develop and maintain SAS programs for data importing, quality assurance, and reporting.

  • Produce Define XML/PDFs, aCRFs, and Reviewers Guides to support SDTMs and ADaMs

SAS Programmer requirements

  • BS in Statistics, Computer Science, Mathematics, or a similar field. Work experience will be considered.

  • Deep knowledge of SAS. Skills in R and Python are a plus.

  • Programming experience in the CRO or Pharmaceutical industry

  • Knowledge of data standards for clinical research and statistical analysis (e.g., CDISC, SDTM, ADaM, ICH Statistical Principles for Clinical Trials)

  • Excellent oral and written communication skills

  • Ability to read, analyze, and interpret complex documents.

  • Strong organization skills and flexibility to respond to changing deadlines.

Biomedical Statistical Consulting is committed to creating an inclusive workplace that promotes and values diversity.