Offer summary
Qualifications:
MS or PhD in biostatistics, statistics, or epidemiology, At least 4 years related experience with MS or 1 year with PhD, Proficiency with SAS and/or R programming, Expertise in statistical methods for clinical research, Experience publishing/presenting methodological research.
Key responsabilities:
- Lead study design collaboration with clinical investigators
- Supervise team members including Biostatisticians and programmers
- Perform statistical analysis and write reports and publications
- Ensure scientific integrity of research projects
- Participate in development of Standard Operating Procedures