This is a full-time permanent opportunity with remote in UK. The Senior Statistician will be responsible for protocol development and statistical analysis plans for assigned studies. Additional tasks include providing statistical oversight to studies and ensuring adequate quality and consistency with project requirements.

The Associate Director, Biostatistics will participate in all biostatistics activities in a clinical development program from clinical design to regulatory submission. Includes clinical trial design, statistical analysis development, carrying out modeling and simulation, and overseeing statistical deliverables.