Job Summary
A company is looking for an Associate Director, Biostatistics.
Key Responsibilities
- Oversee statistical activities for multiple clinical studies and manage statistical efforts
- Contribute to clinical protocol development and author statistical analysis plans
- Provide oversight of CROs for outsourced statistical activities and ensure quality control of results
Required Qualifications
- PhD in statistics or a related field with at least 6 years of relevant clinical trial experience, or MS with at least 9 years
- In-depth knowledge of FDA, EMA, and ICH regulations and guidelines
- Proficient in statistical programming (SAS required, R is a plus)
- Experience with ADaM and SDTM
- Experience with trial design software (e.g., EAST) is preferred
Comments