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    Senior SAS Programmer
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    Experis Manpower Group

    Senior SAS Programmer

    Experis Manpower Group
    Łódź
    Type of work
    Full-time
    Experience
    Senior
    Employment Type
    B2B
    Operating mode
    Remote

    Tech stack

      SAS modules

      advanced

      English

      advanced

      SAS

      advanced

      CDISC standards

      regular

    Job description

    Online interview

    We are seeking an experienced Senior SAS Programmer to join our team. The ideal candidate will have proven expertise in SAS programming, with a strong ability to lead programming efforts for clinical studies and produce high-quality Tables, Listings, and Figures (TLFs).

     

    Responsibilities:

    • Lead SAS programming activities for clinical studies, ensuring adherence to study protocols, statistical analysis plans (SAPs), and regulatory requirements
    • Develop, validate, and maintain SAS programs to generate analysis datasets, TLFs, and other clinical trial deliverables
    • Collaborate closely with cross-functional teams including statisticians, data managers, and clinical operations to ensure timely and accurate deliverables
    • Provide technical guidance and mentorship to junior programmers, ensuring adherence to programming standards and best practices
    • Participate in study team meetings, contributing SAS programming expertise to study design and analysis strategies
    • Contribute to the development and implementation of departmental programming standards and processes to optimize efficiency and ensure quality
    • Ensure compliance with regulatory guidelines (e.g., FDA, ICH) and company SOPs throughout all programming activities

     

    Requirements:

    • Bachelor's degree in Computer Science, Statistics, Mathematics, or a related field; advanced degree preferred
    • Minimum 7 years of hands-on experience in SAS programming within the pharmaceutical, biotechnology, or clinical research industry
    • Proficiency in SAS/Base, SAS/STAT, SAS/Macro, and other relevant SAS modules
    • Demonstrated experience in leading SAS programming efforts for clinical studies, including complex TLFs
    • Strong understanding of CDISC standards (e.g., SDTM, ADaM) and their application in clinical trials
    • Excellent problem-solving skills, attention to detail, and ability to work effectively in a team environment
    • Proven ability to effectively communicate technical concepts to non-technical stakeholders
    • Experience with submission deliverables and familiarity with regulatory requirements (e.g., FDA, EMA) preferred
    • Prior experience in mentoring junior programmers and leading programming teams is desirable

     

    Our offer:

    • Workplace: 100% remote 
    • MultiSport Plus
    • Group insurance
    • Medicover Premium
    • e-learning platform