Statistical Data Specialist - Regulatory Affairs - Itatiba - beBeeSas

    beBeeSas
    beBeeSas Itatiba

    há 3 dias

    Título do emprego: Clinical Statistical Programmer

    Descrição
    Clinical Statistical Programmer Overview

    We are seeking a detail-oriented Clinical Statistical Programmer to play a key role in supporting clinical trial data standardization, statistical analysis, and regulatory submissions.

    Key Responsibilities:
    1. Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets.
    2. Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions.
    The ideal candidate will have strong hands-on experience with SAS programming. A solid expertise in CDISC standards is also required as well as experience generating TLFs for regulatory submissions. Knowledge of Python or R scripting language would be beneficial but not essential. The selected candidate must demonstrate excellent documentation practices throughout the entire process.
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