Biostatistics Sr Assoc (Study Statistician)
Tasks
- Author statistical documents
- Collaborate with programming colleagues
- Conduct endpoint analyses
- Contribute to clinical publications
- Contribute to regulatory submissions
- Contribute to study reports
- Maintain statistical sections of trial master file
- Perform clinical trial statistical analyses
- Perform dataset and output quality control
- Perform exploratory analyses
- Provide statistical input in clinical study team meetings
- Review external supplier deliverables
- Stay current with statistical methodologies and regulatory guidelines
- Support audits
- Support dose level review
- Validate compliance with CDISC standards
Perks/Benefits
Skills/Tech-stack
ADaM | Analysis Plan | CDISC | Clinical Trial Methodology | Clinical trial | Quality Control | R | SAS | SDTM | Statistical Analysis | Statistical Analysis Plan | Statistical programming | Trial methodology
Education
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