Data Science Professional - Clinical Trial Data Standardization - Pelotas - beBeeClinicalStatisticalProgrammer

Título do emprego: Clinical Statistical Programmer

Descrição

Job Title: Clinical Statistical Programmer (SAS / CDISC)

Location: Brazil (Remote)

Duration: Long Term Contract

We are seeking a detail-oriented Clinical Statistical Programmer, responsible for sustaining clinical trial data quality. The ideal candidate will possess strong expertise in CDISC standards, SAS programming, and generation of Tables, Listings, and Figures.

Main Responsibilities:

The programmer must be able to transform complex data from various sources into compliant format using standard operating procedures.,
i{Transforming Data }; ,
• (Develop TLFs for clinical study reports)
The statistician must develop well-documented tables which illustrate the overall trends of trials; A critical aspect is that these should meet regulatory submissions needs. Programmers also have to validate their own code. (