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Biostatistician
Job Summary
A company is looking for a Biostatistician to design, analyze, and interpret clinical trial data supporting drug development and regulatory submissions.
Key Responsibilities:
- Collaborate with clinical and regulatory teams to design statistically sound clinical trials
- Develop and review statistical analysis plans in compliance with regulatory guidelines
- Perform statistical analyses on clinical trial datasets using statistical software
Required Qualifications:
- Master's or Ph.D. in Biostatistics, Statistics, Mathematics, or a related quantitative field
- Minimum of 3 years (for MS) or 1 year (for PhD) of relevant experience in the industry
- Proficient in statistical programming languages such as SAS and/or R
- In-depth knowledge of ICH-GCP, CDISC standards, and regulatory guidance documents
- Strong understanding of clinical trial design and regulatory requirements
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COMPLETE JOB DESCRIPTION
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