Senior Biostatistician
United States-New Jersey-Remote, United States
R
USD 136K-198K (estimate) Senior-level Full Time
Tasks
- Author and review clinical study reports
- Author and review protocols
- Collaborate with clinicians and medical writers
- Conduct statistical methodology research
- Coordinate regulatory submission support
- Develop case report forms
- Develop clinical trial designs
- Drive integrated analyses
- Ensure analyses support hypotheses
- Ensure compliance with SOPs
- Interpret trial results
- Plan statistical analyses
- Prepare data presentation plan
- Prepare statistical analysis plan
- Provide statistical consultation for ad hoc requests
- Support regulatory filings and approvals
- Translate scientific questions to statistical terms
Perks/Benefits
Skills/Tech-stack
Analysis Plan | CDISC | Clinical Trial Design | Clinical data | Clinical data standards | Clinical study | Clinical study reports | Clinical trial | Clinical trials | Clinical trials methodology | Data Presentation | Data Standards | Data summarization | Endpoint selection | Hypothesis Testing | Integrated Analysis | Population Selection | Protocol development | Regulatory Submission | Research Methodology | Statistical Analysis | Statistical Analysis Plan | Statistical Hypothesis Testing | Study Reports | Trial design
Education
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