Offer summary
Qualifications:
Ph.D degree in Statistics or Biostatistics, Experience in the pharmaceutical or biotechnology industry, Good Clinical Practice (GCP) proficient, Advanced knowledge of Biostatistics, Proficient programming skills in R and SAS.
Key responsabilities:
- Accountable for biostatistical activities in clinical studies
- Oversight of vendor biostatistical work for high quality
- Develop statistical analysis plans and review documents
- Provide statistical expertise for protocol development
- Conduct statistical analysis to support clinical decisions