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Principal Biostatistician
Job Summary
A company is looking for a Principal Biostatistician, FSP, Late Phase.
Key Responsibilities
- Collaborate with project teams to establish objectives and timelines
- Write statistical sections of clinical trial protocols and author statistical analysis plans
- Monitor project activities and contribute to clinical study reports and regulatory documents
Required Qualifications
- PhD in Statistics, Biostatistics, or related field with 5+ years of industry experience, or MS with 7+ years
- At least 3 years of Phase 2/3 clinical trial experience
- Proficiency in R or SAS for efficacy and safety analyses
- Understanding of ICH GCP and industry practices
- Experience with CDISC standards, including SDTM and ADAM
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COMPLETE JOB DESCRIPTION
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Company Overview
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