Biostatistics Sr Associate (Study Statistician)
Tasks
- Author statistical analysis plans
- Collaborate with programming colleagues
- Conduct exploratory analyses
- Contribute to clinical publications
- Create randomization specifications
- Create submission data file specifications
- Develop table figure listing shells
- Ensure CDISC compliance
- Maintain trial master file statistical sections
- Participate in clinical study team meetings
- Perform clinical trial endpoint analyses
- Perform dataset quality control
- Provide statistical input
- Review external supplier deliverables
- Stay current on statistical methods and guidelines
- Support regulatory submissions
Perks/Benefits
Skills/Tech-stack
ADaM | CDISC | Clinical Trial Methodology | Clinical trial | Clinical trials | Data Analysis | Quality Control | R | Randomization | SAS | SAS programming | SDTM | Statistical Analysis | Statistical programming | Trial methodology
Education
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