Senior Statistical Programmer - South Africa (Remote)

Mms; Cape Town; Remote; ZAR 500 000 - 700 000; Full time

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

SAS programming

Generating tables from databases

Team leadership

Communication skills

Education

Master's degree

Tools

SAS Base

MS Office

Job description

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.

Job Overview

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).

Job Specific Skills

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.

Job Requirements

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.