**Statistical Programmer Job Opportunity**
This role involves developing and maintaining programs for clinical trial data analysis and reporting. The ideal candidate will have strong SAS programming skills and experience with statistical analysis of clinical trials.
Responsibilities
* Develop datasets (e.g., ADaM) and review study documentation from a programming perspective.
* Create tables, listings, and figures (TLFs) in line with trial protocols and statistical plans.
* Perform quality control (QC) and document results per SOPs.
* Support study teams with data presentation and interpretation.
* Provide input on technical issues and propose solutions.
* Keep programming and documentation up to date and audit-ready.
Qualifications & Experience
* University degree in mathematics, computer science, or a related field.
* Strong knowledge of CDISC standards, especially SDTM and ADaM.
* Basic knowledge of R and other programming languages is a plus.
* At least 4 years of experience in statistical programming, including 3 years in pharma or CRO.
* Familiarity with ICH-GCP and clinical trial regulations.
* Excellent communication skills in English.
Key Requirements
* Job Function: Research and Other
* Industry: Pharmaceutical Manufacturing