Offer summary
Qualifications:
Master's degree in Statistics/Biostatistics, 4+ years of statistical experience in pharmaceutical industry or medical research, Strong SAS and/or R programming skills.Key responsabilities:
- Lead statistical activities of clinical studies
- Collaborate with cross-functional team members
- Provide statistical guidance and review protocols/SAPs/TFLs/DMC Charters
- Perform statistical analysis of studies/projects
- Manage timelines for statistics-related deliverables