Senior / Principal Statistical Programmer (clinical Sas Programmer), South Africa
Parexel
South Africa
Advanced sas programming techniques
Clinical trial data analysis and reporting
Ich-gcp and 21 cfr part 11 regulatory knowledge
The role involves providing technical expertise as a subject matter expert for the conduct of clinical trials and supporting analysis and reporting activities
Job Summary
The role involves providing technical expertise as a subject matter expert for the conduct of clinical trials and supporting analysis and reporting activities.
Candidates must be able to fill the Statistical Programming Lead role, liaising with sponsors, Biostatistics Leads, and Data Management Leads.
The position requires monitoring quality, timelines, resource allocation, and productivity while ensuring compliance with SOPs and international regulations.
Matching Summary
The role involves providing technical expertise as a subject matter expert for the conduct of clinical trials and supporting analysis and reporting activities.
Skills & Requirements
Must-have
Advanced SAS programming techniques
Clinical trial data analysis and reporting
ICH-GCP and 21 CFR Part 11 regulatory knowledge
Statistical programming team leadership experience
Minimum 3.5 to 5 years clinical programming experience
Nice-to-have
Strong project management and resource allocation skills
Ability to mentor global teams effectively
Excellent negotiation and business development skills
Client-focused approach with high quality standards
Adaptability to evolving technical environments
Key Requirements
Degree level education in relevant discipline
Minimum 3.5 years related experience for Senior level
Minimum 5 years with Lead experience for Principal level