Clinical SAS Programmer

Katalyst Healthcares & Life Sciences
South Plainfield, NJ Contractor
POSTED ON 3/18/2024
Responsibilities:
  • Develop, validate, and maintain SAS programs for clinical data analysis, reporting, and submission in adherence to CDISC standards, regulatory guidelines, and company SOPs.
  • Lead the programming activities for regulatory submissions, ensuring timely and accurate delivery of high-quality datasets, tables, listings, and figures (TLFs).
  • Collaborate closely with biostatisticians to generate analysis datasets, perform statistical analyses, and contribute to the interpretation and presentation of study results for submission.
  • Ensure data quality and integrity by conducting thorough quality control (QC) checks and implementing appropriate validation procedures.
  • Provide expertise in CDISC standards (SDTM and ADaM) and contribute to the development and implementation of data standards and submission deliverables.
Requirements:
  • Bachelor's or master's degree in a relevant field such as computer science, statistics, or life sciences.
  • Minimum of 5 years of experience as a SAS programmer in the pharmaceutical or biotechnology industry, with a strong focus on oncology clinical trials and regulatory submissions.
  • Extensive expertise in SAS programming, including data manipulation, analysis, and reporting.
  • Proven experience working with CDISC standards (SDTM and ADaM) and implementing these standards in clinical trials and regulatory submissions.
  • Strong understanding of regulatory guidelines (e.g., FDA, EMA, ICH-GCP) governing the analysis and reporting of clinical trial data for regulatory submissions.
  • Proficiency in statistical programming using SAS, including experience with SAS/Base, SAS/STAT, SAS/Macro, and SAS/Graph.
  • Excellent problem-solving skills, attention to detail, and the ability to work independently in a fast-paced environment.

Hourly Wage Estimation for Clinical SAS Programmer in South Plainfield, NJ
$40.56 to $51.56
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