Job title: Clinical SAS Programmer
Company: Katalyst Healthcares & Life Sciences
Job description: Responsibilities:
- Develop and maintain SAS programs to import, clean, and validate clinical trial data.
- Use R for data manipulation, analysis, and visualization.
- Perform statistical analyses in accordance with study protocols and analysis plans.
- Generate tables, listings, and figures (TLFs) using SAS and R.
- Create and QC statistical outputs and clinical study reports for regulatory submissions.
- Document programming activities and ensure compliance with Standard Operating Procedures (SOPs).
- Work closely with biostatisticians, data managers, and clinical researchers.
- Provide programming support for ad-hoc analysis requests and exploratory data analyses.
- Perform rigorous quality checks on all deliverables.
- Maintain annotated datasets and ensure traceability of data processing.
Requirements:
- Bachelor’s or Master’s degree in Statistics, Computer Science, Biostatistics, or a related field.
- Minimum of 3 years of clinical SAS programming experience, with a strong background in R.
- Proficiency in SAS and R, including data step programming, PROC SQL, and R packages for data analysis.
- Experience with CDISC standards (SDTM, ADaM).
- Knowledge of clinical trial processes and regulatory requirements (e.g., FDA, EMA).
- Strong analytical and problem-solving skills.
- Excellent communication skills, both written and verbal.
Expected salary:
Location: South Plainfield, NJ
Job date: Thu, 12 Sep 2024 03:37:00 GMT
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