- Developing TLFs for clinical study reports and regulatory submissions;
- Writing efficient SAS programs for data cleaning; derivations; reporting;
- Maintaining reusable Python or R scripts for automation; validation; reproducible reporting;
- Performing programming QC with peer reviews to ensure accuracy and traceability.
- A minimum 5 years' experience with SAS programming language including creating software specifications as well as collaborating team members within information technology industry preferred but not required.
Strong knowledge on integration science from acquisition program defining new domain representative possible feedback utilization tool development link.
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Clinical Data Analysis Specialist - Santa Luzia, MG - beBeeDataStandardizer
Título do emprego: Clinical Statistical Programmer
Descrição
Clinical Data Standardization Expert
Role Description:
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).
The successful candidate will be responsible for transforming raw clinical trial data into CDISC-compliant SDTM and ADaM datasets.
Required Qualifications:
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