- Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets
- Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions
- Write efficient SAS programs for data cleaning, derivations, and reporting
- Develop reusable Python or R scripts to support automation validation software development of reproducible code submission reviews require high-quality documentation detail-oriented individual must possess excellent organizational skills communication collaboration building project planning resource allocation implementation execution attention analytical problem-solving critical thinking certification open-source tools table figures source spreadsheet tracking using Microsoft Office Excel offshore recruitment
This position requires strong expertise in SAS programming & CDISC standards (SDTM & ADaM), with experience generating TLFs for
Clinical Data Analyst - Bento Gonçalves - beBeeStatistician
Título do emprego: Clinical Statistical Programmer
Descrição
Clinical Statistical Programmer Position Overview
The ideal candidate will play a key role in supporting clinical trial data standardization, statistical analysis, and regulatory submissions.