Major Responsibilities
1. Coordinate and lead a project team to successful completion of a project within given timelines and budget.
2. Understand and apply advanced statistical methods.
3. Lead production and quality control of randomizations, statistical sections of the protocols, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents.
4. Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques.
5. Check own work in an ongoing way to ensure ***-time quality.
6. Provide training in statistical analysis to internal teams.
7. Mentor and train junior members of the department.
8. Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review.
9. Additional responsibilities as defined by supervisor/manager.

Qualifications
1. Education:
MS or above in Biostatistics, Statistics or related discipline.
2. Minimum Work Experience:
MS in Biostatistics, Statistics or related discipline with 5+ years of experience; PhD in Biostatistics, Statistics or related discipline with 3+ years of experience. Immunology and Oncology experiences preferred.
3. Strategic thinking.
4. Strong communication skills and influence skills.
5. Ability to work within team and work effectively in a changing environment.
6. Critical thinking and problem solving.

Other Requirements
Preference: Knowledge of clinical trials, Immunology and Oncology experiences preferred.
Language Requirements: Competent in written and oral English in addition to local language.
Travel Requirements: None