Offer summary
Qualifications:
Advanced degree in statistics or related field, Experience in clinical trials design and regulatory analysis, Advanced SAS programming experience, Knowledge of CDISC standards, Management experience preferred but not required.
Key responsabilities:
- Supervise and mentor team members
- Provide statistical consulting and support studies
- Prepare statistical analysis plans and documents
- Develop and maintain departmental SOPs
- Contribute to project revenue and costing efforts