Statistical SAS Programmer required to join a team supporting multiple clinical and non clinical studies, particularly focusing on regulatory submissions.

The ideal candidate will be an expert in Study Data Tabulation Model, Analysis Data Model, and other CDISC standards.

Skills
BSc or higher in Computer Science, Mathematics or related subject.
SAS programming within the pharmaceutical industry, with a focus on clinical trials.
Familiarity with regulatory submissions, including associated industry guidance and the application of SDTM and ADaM CDISC standards.
CRT or Case Report Tabulation and define.xml standards.
Developing or managing CRT tools.

Role
Program and validate SDTM datasets, including complex efficacy and lab data, and other clinical outputs.


Technical expert in SDTM, ADaM, and other CDISC standards.

Provide consultancy, advice, and training to the team.
Program complex non efficacy outputs and figures, perform senior review, and deliver quality control of non statistical outputs.
Comply with regulatory guidelines and requirements, particularly related to CDISC standards, GCP (Good Clinical Practice), and clinical trial documentation.