Statistical Programmer II

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

Parexel is hiring for Statistical Programmer II and Senior Statistical Programmer roles as part of our growing Functional Service Provider (FSP) team.

💡 What you’ll do:

• 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.
• Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements.
• Contribute to life-changing research in a flexible, remote-friendly environment

💻 What you’ll bring:

• Proficiency in SAS (Base, Macro, and Graph)
• Sound knowledge of CDISC standards (ADaM, SDTM)
• Proven clinical / statistical programming experience within pharmaceutical clinical development (CRO/Pharma) - Minimum 3years experience is essential
• Strong analytical and communication skills

🌱 What we offer:

• Career growth and mentorship
• Fully remote work options
• A culture of integrity, respect, and innovation

Whether you're advancing your career or bringing senior-level expertise, Parexel empowers you to make a meaningful impact.