Clinical SAS Programmer

Overview

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• Conduct statistical programming and analysis of clinical research studies.
• Provide programming support for publication efforts and regulatory submissions.
• Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects.
• Perform acquisition and curation of data, including full CDISC standardization and Pseudo-CDISC standardization.
• Document and implement programming endpoint algorithms across various projects.
• Review and provide feedback on Statistical Analysis Plans.
• Manage the end-to-end analytics of deliverables from data curation through final presentation, which may include preparation for abstracts and manuscripts.
• Inform internal and external project team members of statistical programming requirements, deliverable status, and resource needs.
• Program clinical research data to facilitate ease of analysis for observational, hypothesis-generating studies.
• Conduct exploratory analyses to support publication and abstract submissions.
• Communicate statistical results to stakeholders to ensure accurate interpretation.

• Master s degree or foreign equivalent in Biostatistics or a related field.
• 6 years of experience as a Statistical Programmer, Clinical Trial Analytics Intern, or a related role within the public health, biomedical, or medical device industries.
• Proficiency in SAS Programming, SAS Macros, R/R Studio, Clinical Trial Design, and Data Analysis.
• Strong analytical and problem-solving skills with attention to detail.
• Ability to work collaboratively in a team environment and communicate effectively with cross-functional teams.
• Excellent organizational skills and the ability to manage multiple tasks and projects simultaneously.

• Mid-Senior level

• Contract

• Information Technology

• Pharmaceutical Manufacturing