Offer summary
Qualifications:
Master's degree / PhD in Statistics, Biostatistics, or related field with 7-10 years experience, Proficiency with SAS and knowledge of industry standards and complex statistical methods.
Key responsabilities:
- Generate randomization schedules, design CRFs, and author statistical analysis plans
- Develop SAS programs, validate datasets, and review output for accuracy
- Mentor junior team members and provide statistical support for clinical trials
- Collaborate with study teams, sponsors, and vendors to ensure project success