Offer summary
Qualifications:
Master's degree or PhD in Statistics, Biostatistics, or related field, At least 7-10 years experience as Biostatistician for Clinical Research Organization, Extensive knowledge of industry standards and SAS, familiarity with complex statistical methods.
Key responsabilities:
- Generate randomization schedules and assist with statistical methods review
- Author statistical analysis plans and validate analysis datasets
- Provide statistical support for supplemental analyses, review statistical sections of clinical study reports
- Mentor and support junior team members, collaborate with sponsors, project managers, and vendors
- Train new biostatisticians, assist with bid defense meetings, and complete statistical activities within timelines