
Senior Clinical Research Statistician
7 days ago
Job Summary
We are seeking a highly skilled Senior Biostatistician to join our team. The ideal candidate will have a strong background in biostatistics, with expertise in clinical trials and statistical analysis.
Key Responsibilities:
Provide statistical input into protocol design, including sample size estimations, key efficacy and safety parameters, endpoints, randomisation, and blinding.
Develop Statistical Analysis Plans (SAPs), detailing methodology, programming procedures, variable definitions, and presentation of data and results for assigned studies.
Collaborate 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.
Support Data Monitoring Committees (DMCs), ensuring appropriate blinding is maintained.
Contribute to the review and development of Standard Operating Procedures (SOPs), work instructions, and new processes.
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:
Competitive remuneration.
Flexible work environment, with hybrid and fully remote options.
Ongoing opportunities for learning and development.
Opportunity to work on challenging projects and contribute to the growth and success of the company.
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