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.