Biostatistical Programming Senior Associate
Tasks
- Act as study programmer
- Create randomization lists
- Deliver randomization lists per specifications
- Develop and review GRB policies manuals SOPs
- Execute IRT data transfers into secure sFTP locations
- Maintain documentation for randomization and blinding
- Maintain study blind per SOPs
- Manage IRT data transfer activities
- Participate in cross functional training and presentations
- Respond to audit questions
- Support audits for randomization and blinding
- Understand and execute department study macros and utilities
- Validate randomization assignments
- Verify dose decisions
- Verify dosing algorithms
- Verify electronic systems for randomization schedules
- Write SAS programs for randomization validation
Perks/Benefits
- N/A
Skills/Tech-stack
Blinding | Clinical trials | IRT | Macro | Process Improvement | Project Management | Project Planning | Python | R | Randomization | SAS | SFTP | Statistical programming | Unix | Utility programming
Education
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