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Sas Programmer

0-2 years
Not Disclosed
10 Jan. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: SAS Programmer I (0-2 years of experience)
Location: [Location not provided]
Employment Type: [Employment type not specified]
Job Category: [Category not specified]
Job Number: [Job number not provided]
Is Job Remote?: [Remote status not specified]
Country: United States


Job Overview

The SAS Programmer I role is intended for entry-level professionals with 0-2 years of experience in programming with SAS software. This position involves writing, testing, and optimizing SAS programs to support clinical data analysis for clinical trials. The programmer will work under the guidance of senior team members and gain valuable experience in data management and clinical research.

Essential Job Responsibilities

  • Write and execute SAS programs to clean, analyze, and summarize clinical trial data in compliance with study protocols and regulatory standards.
  • Support the creation of datasets for statistical analysis, including raw data transformations and programming for tables, listings, and figures.
  • Perform data validation checks to ensure the accuracy and integrity of clinical data.
  • Assist in the preparation of analysis datasets, ensuring adherence to CDISC (SDTM, ADaM) standards.
  • Participate in the development of programming specifications and documentation for clinical trial data analysis.
  • Collaborate with other clinical data team members, including biostatisticians and clinical data managers, to ensure the accuracy of the data and the results.
  • Provide support for regulatory submissions, including the preparation of datasets for submission to the FDA and other regulatory bodies.
  • Ensure that programming tasks are completed on time and meet quality standards.
  • Develop proficiency in SAS programming techniques, troubleshooting, and debugging SAS code.

Required Qualifications

  • Bachelor’s degree in Computer Science, Statistics, Life Sciences, or a related field.
  • 0-2 years of experience in SAS programming, ideally in the clinical research or pharmaceutical industry.
  • Basic knowledge of clinical trial processes and regulatory requirements (e.g., ICH GCP, CDISC).
  • Proficiency in SAS programming, including data step processing, PROC procedures, and macros.
  • Familiarity with statistical analysis concepts and data management.
  • Ability to troubleshoot and optimize SAS code.
  • Strong attention to detail and the ability to maintain data integrity.
  • Excellent problem-solving, communication, and teamwork skills.

Preferred Qualifications

  • Experience with clinical data management systems (CDMS) or electronic data capture (EDC) systems.
  • Familiarity with CDISC data standards (SDTM, ADaM).
  • Experience with additional programming languages such as R or Python is a plus.

Additional Information

[Additional company and diversity-related information, if applicable.]