Senior SAS Programmer – Clinical Trials & Submissions

Mms Holdings Inc.; Remote; ZAR 600 000 - 800 000; Full time

Job summary

A leading clinical research organization in Pretoria seeks an experienced Senior Statistical Programmer to lead programming project teams. The role demands mastery in SAS programming and a strong understanding of regulatory submissions. Candidates should have a Master's degree in Statistics and at least 5 years of experience in statistical programming. The organization promotes a collaborative environment and exceptional employee support aimed at shaping the future of clinical research.

Qualifications

• Minimum of 5 years' experience in Statistical Programming or similar field.
• Hands-on experience with clinical trial and pharmaceutical development preferred.
• Good communication and organizational skills.
• Familiarity with FDA and GCP requirements.

Responsibilities

• Lead study or small programming project teams.

Skills

SAS programming

E-Submission Standards knowledge

SDTM standards

ADaM standards

MS Office

ICH guidelines

BIMO outputs knowledge

Education

Master's degree in Statistics

Job description

A leading clinical research organization in Pretoria seeks an experienced Senior Statistical Programmer to lead programming project teams. The role demands mastery in SAS programming and a strong understanding of regulatory submissions. Candidates should have a Master's degree in Statistics and at least 5 years of experience in statistical programming. The organization promotes a collaborative environment and exceptional employee support aimed at shaping the future of clinical research.