Penfield Search Partners
Contact: Neisha Camacho/Terra Parsons – teamnt@penfieldsearch.com
Job Description: The SAS Programmer is 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 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
Qualifications:
- 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.