Job Summary
A company is looking for a Principal Biostatistician to join their Biostatistics team.
Key Responsibilities
- Lead biostatistical activities for clinical trial projects, providing expert statistical input and consultancy
- Generate and validate clinical trial deliverables, ensuring quality control and supervising SAS programming
- Develop and review statistical documentation, including analysis plans and specifications for data sets
Required Qualifications
- Advanced degree (MS or PhD) in statistics or a closely related field
- 12-15 years of experience in clinical trials design and analysis
- Expert knowledge of clinical trial design principles and advanced statistical concepts
- Strong programming skills, particularly in statistical inferential procedures
- Experience interacting with regulatory agencies (e.g., FDA, EMA)
Comments