Remote Statistical Programmer II – CDISC & Trial Analysis

Parexel International; Remote; ZAR 300 000 - 400 000; Full time

Job summary

A leading clinical research organization is looking for a Statistical Programmer II who will develop and validate SAS programs for clinical trial datasets. The ideal candidate will have at least 3 years of experience in clinical/statistical programming in the pharmaceutical field and be proficient in SAS. With fully remote work options, this role offers a chance to contribute to life-changing research and advance your career.

Benefits

Career growth and mentorship

Flexible remote work options

Culture of integrity, respect, and innovation

Qualifications

• Minimum 3 years of clinical/statistical programming experience in pharmaceutical clinical development.
• Knowledge of CDISC standards (ADaM, SDTM) is essential.

Responsibilities

• Develop and validate SAS programs for datasets, tables, listings, and figures.
• Collaborate with global teams to support clinical trial analysis.
• Ensure compliance with CDISC standards and regulatory requirements.
• Support the electronic submission preparation and review.

Skills

Proficiency in SAS (Base, Macro, and Graph)

Strong analytical and communication skills

Job description

A leading clinical research organization is looking for a Statistical Programmer II who will develop and validate SAS programs for clinical trial datasets. The ideal candidate will have at least 3 years of experience in clinical/statistical programming in the pharmaceutical field and be proficient in SAS. With fully remote work options, this role offers a chance to contribute to life-changing research and advance your career.