Ontshikile Willington Moalosi
Statistical Programmer I
Bloemfontein,FS
Summary
Meticulous Statistical Programmer I with experience supporting clinical trial analysis and reporting through development of high-quality datasets, tables, figures, and listings. Proficient in programming and validating SDTM and ADaM datasets, ensuring compliance with industry standards and regulatory requirements. Adept at using efficient programming techniques to optimize workflow and enhance data integrity. Ensures quality via meticulous validation and best practices.
Overview
3
3
years of professional experience
2
2
Certifications
3
3
Languages
Work History
Statistical Programmer I
Bristol Myers Squibb
04.2025 - Current
- Developed and validated statistical programming algorithms to ensure data integrity and compliance with regulatory standards.
- Collaborated with cross-functional teams to design and implement Tables Listings and Figures
- Executed data cleaning and transformation processes, resulting in improved accuracy and reliability of datasets for analysis.
- Support programming activities for analysis and reporting of clinical study data under supervision.
- Develop and validate SDTM and ADaM datasets, ensuring compliance with CDISC and regulatory standards.
- Check own work in an ongoing way to ensure first-time quality.
- Use efficient programming techniques to produce derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings and QC low-medium complexity derived datasets, tables, figures, and data listings.
- Assist in the production/QC of derived dataset specifications and other process supporting documents and submission documentation.
- Utilized SAS and SAS Macro Language and SAS SQL programming languages to analyze clinical trial data, ensuring adherence to industry protocols.
Statistical Programmer I
Parexel International
05.2022 - Current
- Support programming activities for analysis and reporting of clinical study data under supervision.
- Develop and validate SDTM and ADaM datasets, ensuring compliance with CDISC and regulatory standards.
- Check own work in an ongoing way to ensure first-time quality.
- Use efficient programming techniques to produce derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings and QC low-medium complexity derived datasets, tables, figures, and data listings.
- Assist in the production/QC of derived dataset specifications and other process supporting documents and submission documentation.
- Utilized SAS and SAS Macro Language and SAS SQL programming languages to analyze clinical trial data, ensuring adherence to industry protocols.
Education
Diploma - Information Technology
Central University of Technology
01.2021
Higher Certificate - Information Technology
CTI Education Group
01.2014
Skills
- Proficient in SDTM and ADaM programming
- TLF Development & Validation
- SAS Programming & Macro Language
- Experience in SQL within SAS environment
- Data mapping and validation
- CDISC standards expertise
Certification
SAS Macro Language – SAS Institute
References
- Ruan, Foord, Statistical programmer, Ruan.Foord@parexel.com, +27 81 766 7773, Parexel
Timeline
Statistical Programmer I
Bristol Myers Squibb
04.2025 - Current
Statistical Programmer I
Parexel International
05.2022 - Current
Higher Certificate - Information Technology
CTI Education Group
Diploma - Information Technology
Central University of Technology