Offer summary
Qualifications:
MS or PhD in biostatistics, statistics, or epidemiology., At least 4 years related experience with MS or 1 year with PhD., Strong programming skills in SAS and/or R., Demonstrated proficiency with statistical methods in clinical research..Key responsabilities:
- Lead collaborations on study design and protocol development.
- Supervise Biostatisticians and SAS programmers, review statistical designs.