Senior Biostatistician
USA IRV-17011 Redhill/DBC1-5, United States
USD 119K-168K Senior-level Full Time
Tasks
- Author clinical study reports
- Conduct literature reviews and attend professional meetings
- Develop case report forms and clinical databases
- Develop statistical analysis plans
- Ensure data quality
- Generate study randomization schemes
- Lead statistical analysis efforts
- Participate in study team discussions
- Provide statistical input for regulatory submissions
- Review study protocols and contribute to statistical sections
- Validate statistical content in study documents
Perks/Benefits
- N/A
Skills/Tech-stack
Bayesian Methodology | Biostatistics | Clinical Trial Design | Clinical trial | Data Analysis | R | Regression Analysis | Regulatory Guidelines GCP ICH FDA ISO | Regulatory guidelines | Regulatory guidelines (GCP | SAS | Statistical programming | Statistics | Trial design
Education
Roles
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