Manager, Statistical Programming
Tasks
- Communicate programming issues with project leadership
- Comply with regulatory requirements and SOPs
- Design clinical trial programming solutions
- Develop and implement programming strategies standards and specifications
- Develop robust programming specifications
- Ensure quality of analysis and reporting deliverables
- Evaluate candidates and support onboarding
- Improve efficiency and standardize processes standards and tools
- Integrate analyze and report clinical data
- Provide technical guidance to vendors
- Review data presentation plan and data review plan
- Review protocol and statistical analysis plan
- Support vendor deliverable acceptance
Perks/Benefits
- N/A
Skills/Tech-stack
Clinical Data Analysis | Clinical Trial Methodology | Clinical data | Clinical trial | Cross-functional | Cross-functional teamwork | Data Analysis | Data Presentation | Data review | Global Regulatory Filings | Programming specifications | Regulatory filings | Regulatory requirements | SAS | SAS Base | SAS Graph | SAS Stat | Statistical programming | Trial methodology | Vendor management
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
Roles
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