Lead clinical trial analysis with SAS and R as a Senior Biostatistician in Kimberley, Northern Cape, ZA, under a hybrid work model.

This senior position supports a contract research organization serving global pharmaceutical and biotech companies. You will apply biostatistics across clinical research, supporting regulatory submissions and research objectives. The work combines statistical planning, analysis, interpretation, and reporting.

Key Responsibilities:

- Develop Statistical Analysis Plans with clinical and regulatory teams
- Design clinical trial datasets and specify analysis requirements
- Analyze trial data using SAS and R software
- Interpret results for informed clinical decision-making
- Prepare reports, submissions, and publication statistical sections

Requirements:

- Master's or PhD in Statistics, Biostatistics, or related field
- Five to seven years' pharmaceutical, biotechnology, or CRO experience
- SAS proficiency required; R proficiency preferred
- Understanding of trial design, data management, and ICH E9
- Experience analyzing various clinical trial phases

Apply senior biostatistical expertise in SAS, R, clinical trials, and regulatory reporting from Kimberley’s hybrid setting.

📌 Senior Clinical Trial Biostatistician (Canada)
🏢 Placements24
📍 Canada