Assoc Principal Scientist Statistical Programming, Late-Stage (Hybrid)
USA - New Jersey - Rahway, United States
R
USD 142K-224K Senior-level Full Time
Tasks
- Comply with global and TA reporting standards
- Coordinate global programming team activities
- Create safety and efficacy analysis datasets
- Design and maintain statistical databases
- Develop and execute statistical analysis deliverables
- Develop statistical programming algorithms
- Ensure deliverable quality and process compliance
- Lead programming project planning and resource forecasting
- Prepare electronic regulatory submission deliverables
- Produce tables listings figures and graphics
- Provide technical guidance and mentorship
- Serve as statistical programming point of contact
Perks/Benefits
- N/A
Skills/Tech-stack
ADaM | CDISC | Clinical Trial Data | Clinical trial | Data Management | Data Modeling | Data steps | Electronic Regulatory Submissions | Microsoft Project | Numerical analysis | Project Management | Regulatory Submissions | Relationship Management | SAS | SAS Graph | SAS Macro | SDLC | Stakeholder relationship | Stakeholder relationship management | Statistical Analysis | Statistical Databases | Trial data | Waterfall model
Education
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