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Sas Programmer I

0-2 years
Not Disclosed
10 Jan. 23, 2025
Job Description
Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates 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

Job Title: SAS Programmer I

Experience Required: 0 – 2 Years

Location: [Specify Location]

Job Description:

We are seeking a detail-oriented and motivated SAS Programmer I to join our team. This is an entry-level role suitable for individuals with 0 to 2 years of experience in programming, particularly using SAS for clinical data analysis. As a SAS Programmer I, you will be responsible for supporting data analysis efforts by writing and maintaining SAS programs for clinical trials, ensuring that the data is properly formatted and meets the requirements for regulatory submission.

Key Responsibilities:

  • Write and maintain SAS programs to clean, analyze, and report clinical trial data.
  • Perform data manipulation, analysis, and reporting in accordance with clinical trial specifications and regulatory requirements.
  • Assist in the creation of datasets, tables, listings, and figures for clinical trial reports.
  • Ensure that all programming outputs are accurate, complete, and meet the standards for quality and compliance.
  • Collaborate with the clinical team, including data managers and statisticians, to ensure that data requirements are met.
  • Participate in the review of specifications, data review, and validation to ensure programming accuracy.
  • Adhere to project timelines and deliverables while ensuring that all work complies with ICH-GCP guidelines and regulatory requirements.
  • Troubleshoot programming issues and work to resolve them in a timely and efficient manner.
  • Ensure that all documentation of programming tasks, processes, and outputs is clear and organized.

Qualifications:

  • Bachelor’s degree in Computer Science, Life Sciences, Statistics, Mathematics, or a related field.
  • 0-2 years of experience in SAS programming, preferably in a clinical research or pharmaceutical setting.
  • Basic understanding of SAS programming, statistical analysis, and clinical trial data.
  • Knowledge of clinical trial processes and data management is a plus.
  • Proficiency in SAS, with knowledge of SAS procedures and functions.
  • Familiarity with CDISC standards, SDTM, and ADaM is desirable.
  • Strong analytical skills with attention to detail.
  • Ability to work effectively both independently and as part of a team.
  • Good communication skills, with the ability to collaborate with cross-functional teams.
  • Willingness to learn and develop programming skills in a clinical research environment.

This is an excellent opportunity for an entry-level SAS programmer to gain hands-on experience in clinical data programming and analysis. If you have a passion for programming and want to contribute to clinical research efforts, we encourage you to apply.

Rush your CVs to : careers@clinztech.com