Principal Biostatistician
USA IRV-1411 McGaw Ave/LINC, United States
USD 132K-186K Senior-level Full Time
Tasks
- Advise on clinical study conduct
- Analyze clinical endpoints
- Collaborate on regulatory submissions
- Compile technical documents for audits
- Conduct survival analysis
- Coordinate analyses for study report and documents
- Develop case report forms
- Develop statistical analysis plans
- Ensure data quality assurance
- Lead clinical trial statistical analyses
- Provide SAS programming and validation support
- Represent biostatistics on clinical development teams
- Support clinical database development
- Support data monitoring committee analyses
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | Case Report Form | Case Report Form Development | Clinical Trial Design | Clinical endpoints | Clinical trial | Data Management | Data Quality | Data quality assurance | FDA | Form development | GCP | ICH | ISO | Programming validation | Quality Assurance | R | Regulatory Submissions | Report/form development | SAS | Splus | Statistical Analysis | Statistical Analysis Plan | Statistical modeling | Survival analysis | Trial design
Education
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