Biostatistician II
Site Kansas - 10103 Metcalf Ave, United States
USD 70K-90K Mid-level Full Time
Tasks
- Answer regulatory deficiency letters
- Coordinate delivery of clinical trial documents
- Create inferential statistical programs in SAS
- Create summary tables and graphics
- Develop TFL shells
- Develop and QC review statistical analysis programs
- Develop statistical analysis plans
- Ensure compliance with SOPs and GCP
- Generate randomization schedules
- Independently lead studies
- Maintain regulatory guideline awareness
- Oversee preclinical projects
- Participate in quality improvement initiatives
- Perform QC review of analyses and documents
- Review protocols
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | Clinical Practice | Clinical trials | Data Visualization | Good Clinical Practice | Microsoft Excel | Microsoft Outlook | Microsoft PowerPoint | Microsoft Teams | Microsoft Word | Pharmacodynamics | Pharmacokinetics | Quality Control | Randomization | SAS | SAS programming | Statistical Analysis | Statistical Analysis Plan | Summary Tables
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
Roles
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