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
- Robust 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.

📌 Clinical Research Statistical Analysis Lead (Kimberley)
🏢 Placements24
📍 Kimberley