Job Summary
A company is looking for an Associate Director, Biostatistics.
Key Responsibilities
- Develops study protocols and statistical analysis plans (SAPs) for clinical trials
- Collaborates with teams to ensure data quality and compliance with analysis requirements
- Analyzes clinical trial data and prepares reports to communicate results to project teams
Required Qualifications
- PhD in Statistics or related field with 4+ years of clinical drug development experience, or a Master's with 6+ years of experience
- Knowledge of SAS and/or R is strongly desirable
- Experience with clinical trials and understanding of regulatory guidance are required
- Oncology experience is preferred but not required
- Demonstrated ability to work independently and within a team
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