Clinical Data Science Specialist - Propriá - beBeeDataStandardizer

    beBeeDataStandardizer
    beBeeDataStandardizer Propriá

    há 2 dias

    Título do emprego: Clinical Statistical Programmer

    Descrição

    We are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions.

    Key Responsibilities:

    • Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions
    • Write efficient well-documented SAS programs for data cleaning derivations reporting Python or R scripts automation validation reproducible reporting

    A strong attention to detail documentation practices knowledge of clinical trial data structures submission processes experience supporting FDA EMA regulatory submissions prior experience in a Pharma Biotech CRO environment.

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