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r sas biostatistics clinical trials cdisc📋 Description
- Provide statistical support for Phase I–IV clinical trials.
- Contribute to protocol development, study design, and sample size calculations.
- Prepare and review SAPs, TLF shells, and randomization specs.
- Perform statistical analyses and interpret study results.
- Collaborate with Clinical Data Management, Statistical Programming, and Medical Writing.
- Review outputs, tables, listings, and figures for accuracy and consistency.
🎯 Requirements
- Master’s or PhD in Statistics, Biostatistics, Mathematics, or related field.
- Minimum 5–8 years of experience in biostatistics within CRO/pharma/biotech.
- Strong knowledge of clinical trial methodology and statistical principles.
- Experience with SAS and/or R programming.
- Familiarity with CDISC standards (SDTM/ADaM).
- Experience supporting regulatory submissions is preferred.
🎁 Benefits
- Opportunity to work with a global CRO and sponsor.
- Career development and training opportunities.
- Global footprint across Americas, Europe, and Asia-Pacific.
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