Shape clinical research evidence through statistical analysis and reporting for a leading CRO serving global pharmaceutical and biotech companies.
As Senior Biostatistician, you will contribute to clinical trial design, analysis, and reporting from Kimberley, Northern Cape, ZA. The hybrid work model supports collaboration and focused individual contribution. Your expertise will help maintain statistical integrity and support regulatory submissions.
Key Responsibilities: Participate in study design and protocol development meetings
Develop SAPs for clinical trials with relevant experts
Validate statistical programs and review analytical outputs
Interpret statistical findings and provide decision-making insights
Prepare clinical study reports and regulatory submissions
Requirements: Master's or PhD in a quantitative discipline
Minimum five to seven years as a Biostatistician
Experience within pharmaceutical, biotechnology, or CRO settings
Solid SAS skills and preferred R experience
Excellent analytical, communication, and critical-thinking abilities
Use clinical research expertise, statistical software, and clear communication to strengthen trial evidence and regulatory documentation.

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📌 Clinical Research Statistical Analysis Lead (British Columbia)
🏢 Placements24
📍 British Columbia