Director, Statistical Programming
Location: Wilmington, United States
USD 177K-266K (estimate) Executive-level Full Time
Tasks
- Allocate resources and prioritize programming work
- Collaborate with biostatistics and data management
- Coordinate with clinical operations pharmacovigilance and other functions
- Create analysis tables listings figures graphs
- Develop and validate programming specifications
- Ensure compliance with SOPs
- Ensure study documentation audit readiness
- Generate analysis datasets
- Maintain programming infrastructure
- Manage budgets and forecasts
- Manage programming team performance reviews and mentoring
- Oversee statistical programming activities for clinical studies
- Provide secondary reviews of deliverables
- Support electronic submission in eCTD format
Perks/Benefits
Skills/Tech-stack
21 CFR | 21 CFR Part 11 | Budget Forecasting | CDISC ADaM | CDISC SDTM | CFR Part 11 | Clinical data | Clinical data management | Clinical trial | Clinical trial protocols | Data Management | ECTD | Financial Management | Part 11 | Pharmacovigilance | Project Management | Relational databases | Resource Management | SAS | Scope management | Trial Protocols
Education
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