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Sas Programmer I

0-2 years
Preferred by Companyr
10 Feb. 11, 2025
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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 Level: 0-2 Years

Application Email: careers@clinztech.com


Job Summary

ClinzTech is looking for a motivated SAS Programmer I to join our dynamic team. This entry-level position is ideal for individuals with 0-2 years of experience in SAS programming and clinical data analysis. The selected candidate will be responsible for supporting statistical programming activities for clinical trials, ensuring high-quality data processing and analysis in compliance with industry standards (CDISC, SDTM, ADaM).

This is an excellent opportunity for recent graduates or early-career professionals looking to grow in clinical programming and biostatistics.


Key Responsibilities

SAS Programming & Data Processing

  • Develop, test, and execute SAS programs to analyze and manage clinical trial data.
  • Perform data cleaning, validation, and transformation using SAS Base, SAS Macros, and SAS SQL.
  • Generate tables, listings, and figures (TLFs) for clinical study reports (CSRs).

CDISC Compliance & Data Standards

  • Assist in implementing CDISC standards (SDTM, ADaM) for regulatory compliance.
  • Support the creation of define.xml, annotated CRFs, and metadata documentation.
  • Ensure data integrity and standardization for regulatory submissions (FDA, EMA).

Collaboration & Documentation

  • Work closely with biostatisticians, data managers, and clinical teams to ensure accurate reporting.
  • Maintain detailed documentation of programming activities and data specifications.
  • Support quality control (QC) checks and troubleshoot programming issues.

Qualifications & Requirements

Education:

  • Bachelor’s or Master’s degree in Statistics, Computer Science, Life Sciences, Mathematics, or a related field.

Experience:

  • 0-2 years of experience in SAS programming for clinical trials or healthcare analytics.
  • Knowledge of Electronic Data Capture (EDC) systems (Medidata Rave, Oracle Clinical) is a plus.

Technical Skills:

  • Proficiency in SAS programming (SAS Base, SAS Macro, SAS SQL).
  • Understanding of clinical trial data structures and CDISC standards (SDTM, ADaM).
  • Familiarity with data visualization tools (Tableau, Power BI) and SQL is a plus.

Soft Skills:

  • Strong analytical and problem-solving skills.
  • Ability to work independently and in a team environment.
  • Good written and verbal communication skills.

Preferred Qualifications

  • Internship or coursework experience in biostatistics or clinical programming.
  • Basic understanding of regulatory requirements for clinical trials (FDA, EMA, ICH-GCP).

Benefits & Growth Opportunities

  • Competitive entry-level salary with performance-based bonuses.
  • Comprehensive health, dental, and vision insurance.
  • Opportunities for career advancement and SAS certifications.
  • Mentorship and training programs from experienced industry professionals.
  • A collaborative work environment with exposure to cutting-edge clinical research.

How to Apply

Interested candidates should email their CVs to careers@clinztech.com with the subject line: SAS Programmer I Application – [Your Name].

For more information about ClinzTech, visit Company Website.