Senior Biostatician

Biostatistician Role
We are seeking an experienced Biostatistician to join our team. The ideal candidate will have a strong background in biostatistics and clinical trials, with excellent analytical and problem-solving skills.
About the Role
Develop statistical analysis plans (SAPs) and provide statistical input into protocol design, including sample size estimations and key efficacy and safety parameters.
Provide mentoring and training support to less experienced biostatisticians as required.
SAS programming and related activities to support project deliverables.
Review and QC of statistical outputs produced by Statistical Programmers, ensuring accuracy and clarity in Tables, Listings, and Figures.
Manage statistical service deliverables across assigned projects.
Collaborate effectively with Medical Writers, Project Managers, and other stakeholders to produce high-quality statistical/clinical study reports.
Ensure all analytical programmes are properly documented and validated.
Provide statistical input into the design and review of Case Report Form (CRF) formats.
Actively participate in project team meetings and maintain close liaison with Project Managers.
Support Data Monitoring Committees (DMCs), ensuring appropriate blinding is maintained.
Identify and address operational or quality issues, proposing effective solutions.
Requirements
MSc degree or higher in a statistics related field.
A minimum of 3 years experience in biostatistics, ideally within a CRO environment.
Expert knowledge in biostatistics in clinical trials and the necessary skills to evaluate current programming and other processes, develop strategies for improvement, and execute on those strategies.
Benefits
We offer flexible work arrangements, ongoing opportunities for learning and development, and a safe, inclusive, and respectful workplace where everyone feels valued and empowered to contribute.