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Senior Statistical Programmer - South Africa (Remote)
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Senior Statistical Programmer - South Africa (Remote)
Job summary
A data-focused clinical research organization is seeking a Senior Statistical Programmer to work remotely from South Africa. You will generate pivotal statistical outputs from clinical trial databases using SAS and lead small programming project teams. The ideal candidate holds a Master’s degree and has at least 5 years of relevant experience in statistical programming, demonstrating strong leadership and communication skills.
Qualifications
- Master's degree required.
- Minimum of 5 years' experience in Statistical Programming or a related field.
- Expert knowledge of scientific principles and concepts.
- Strong communication skills and ability to collaborate.
Responsibilities
- Generate tables, listings, and graphs from clinical trial databases using SAS.
- Support regulatory submissions across the SDLC.
- Lead study or small programming project teams.
Skills
Education
Tools
Senior Statistical Programmer - South Africa (Remote) MMS is an award-winning, data-focused clinical research organization that supports the pharmaceutical, biotech, and medical device industries across four continents.
We are looking for a senior statistical programmer to generate tables, listings, and graphs from clinical trial databases using SAS and support regulatory submissions, operating within the System Development Life Cycle (SDLC).
Mastery in generating tables, listings, and graphs from clinical trial databases using SAS.
Proficient in SAS Base, SAS Macros, and advanced SAS programming.
Advanced knowledge of E-Submission Standards, Guidelines and Regulations.
Mastery of SDTM standards and experience writing specifications.
Advanced knowledge of ADaM standards and supporting specification writing.
Proficient with MS Office applications.
Advanced knowledge of ICH, 21CRF Part 11, and ISO
Experience with pooling of data sets for submissions.
Experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP.
Lead study or small programming project teams.
Master's degree required.
Minimum of 5 years' experience in Statistical Programming or a related field.
Expert knowledge of scientific principles and concepts.
Emerging leader with sustained performance and accomplishments.
Proficiency with MS Office applications.
Hands‑on experience with clinical trial and pharmaceutical development preferred.
Strong communication skills and ability to collaborate to solve problems.
Excellent problem‑solving skills.
Good organizational and communication skills.
Familiarity with ISO
Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
Basic understanding CROs and the drug development process.
Should you not receive a response within 14 days of application, your application may be considered unsuccessful.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.