Clinical Programmer

in Healthcare + Life Sciences
  • Bedford, Massachusetts View on Map
  • Salary: $68.00 - $68.00
Contract

Job Detail

  • Experience Level Mid Level
  • Degree Type Bachelor of Science (BS)
  • Employment Contract
  • Working Type Remote
  • Job Reference 0000018120
  • Salary Type Hourly
  • Industry Pharmaceuticals
  • Selling Points

    Contribute to impactful clinical programming projects in a remote contract role. Enhance your SAS programming expertise while collaborating with industry professionals. Gain valuable experience in Pharma/Biotech data management.

Job Description

Overview

  • Develop and validate SAS programs to generate data review, cleaning, and reconciliation listings for clinical studies.
  • Create listings, tables, profiles, figures, and datasets per industry standards and specifications.
  • Execute and debug existing SAS programs, resolving errors and implementing improvements.
  • Perform user administration in EDC systems using established templates and best practices.
  • Develop and apply SAS macros and SQL to enhance programming efficiency.
  • Conduct data mappings between sources and outputs using annotated CRFs and industry standards.
  • Develop data visualization packages and perform data reconciliation as required.
  • Collaborate with data managers and study teams to resolve data issues and ensure quality.
  • Maintain detailed documentation of programming activities and validation processes.

Key Responsibilities & Duties

  • Develop SAS programs for clinical data review, cleaning, and reconciliation tasks.
  • Generate and validate listings, tables, figures, and datasets per specifications.
  • Execute existing programs, debug issues, and implement enhancements.
  • Perform EDC user administration and apply SAS macros for efficiency.
  • Conduct data mappings and quality checks using annotated CRFs.
  • Develop visualization packages and reconcile data as needed.
  • Collaborate with study teams to resolve data issues and ensure deliverables.
  • Assist in statistical programming activities and perform quality control checks.
  • Document programming activities and validation processes comprehensively.

Job Requirements

  • Bachelor’s degree in scientific, biological, statistical, or computer science field required.
  • Minimum 5 years of experience in Pharma/Biotech SAS programming; 8 years preferred.
  • Proficiency in SAS programming and familiarity with CDISC/CDASH and SDTM standards.
  • Strong analytical, problem-solving, organizational, and communication skills.
  • Experience with data mappings, reconciliation, and visualization development.
  • Ability to perform quality checks and resolve data consistency issues.
  • Knowledge of industry best practices and regulatory standards.
  • SAS certification and familiarity with statistical programming preferred.
  • Adaptability, integrity, and accountability in independent and team settings.
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