- Key Responsibilities
- 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, well-documented SAS programs for data cleaning, derivations, and reporting
- Develop reusable Python or R scripts to support automation validation [/code]
Statistical Data Analyst - Clinical Trials Specialist - Jaboatão dos Guararapes, PE - beBeeClinicalStatistician
Título do emprego: Clinical Statistical Programmer
Descrição
Job Title: Clinical Statistical Programmer (SAS / CDISC)