- Possess hands-on experience with SAS programming
- Strong understanding of CDISC standards (SDTM & ADaM)
- Familiarity with TLFs for regulatory submissions
- Knowledge of clinical trial data structures and submission processes
- Attention to detail is crucial, as well as excellent documentation practices
Clinical Data Science Specialist - Caxias do Sul - beBeeSASProgrammer
Título do emprego: Clinical Statistical Programmer
Descrição
Clinical Statistical Programmer Role Overview
We are seeking a highly skilled Clinical Statistical Programmer to support the standardization, analysis, and regulatory submission of clinical trial data. The ideal candidate will have strong expertise in CDISC standards (SDTM & ADaM), SAS programming, and generation of Tables, Listings, and Figures (TLFs). Additionally, experience in quality control and submission readiness is essential.
Required Skills and Qualifications:
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