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Principal Biostatistician
1 month ago
**Operational Execution**
Provide broad statistical support, including trial design, protocol and CRF development on specific studies
Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
Perform sample-size calculations, generate randomization lists and write statistical methodology sections for inclusion in study protocols
Provide statistical input into Data Monitoring Committee (DMC) activities, including development of DMC charters and analysis plans
Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review
**General Activities**
**Knowledge and Experience**:
PhD or MS in Statistics or related discipline with substantial experience around 6+ Years The knowledge of pharmacokinetic data is an advantage Competent in written and oral English in addition to local language
**Education**:
PhD in Statistics or related discipline, MS in Statistics or related discipline
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