Manager - Statistical Programming
Tasks
- Comply with regulatory requirements and SOPs
- Coordinate with cross functional teams on project issues
- Create robust programming specifications for internal and external work
- Design programming solutions for clinical data integration
- Develop and implement clinical trial programming strategies
- Develop programming standards specifications and analysis programs
- Ensure quality of deliverables using A and R standards
- Evaluate candidates and support onboarding
- Improve efficiency through process standardization and tools
- Provide guidance to vendors for programming conventions and file transfers
- Review data presentation plan and data review plan
- Review protocol and statistical analysis plan
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | Clinical Data Analysis | Clinical Reporting | Clinical Trial Methodology | Clinical data | Clinical data integration | Clinical trial | Cross-Functional Collaboration | Cross-functional | Data Analysis | Data Presentation | Data Presentation Plan | Data Review Plan | Data integration | Data review | Functional collaboration | Global Regulatory Affairs | Protocol | Regulatory Affairs | SAS | SAS Base | SAS Graph | SAS Stat | SOP compliance | Statistical Analysis | Statistical Analysis Plan | Trial methodology | Vendor management
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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