Associate Director, Statistical Programming
Tasks
- Collaborate on programming specifications
- Contribute to regulatory submissions
- Develop and validate datasets and reports
- Develop macros and tools
- Ensure compliance with regulatory standards
- Lead statistical programming activities
- Manage CROs and contractors
- Mentor and develop programming staff
- Oversee programming deliverables and timelines
- Represent programming in audits and inspections
Perks/Benefits
Skills/Tech-stack
ADaM | CDISC | Clinical Trial Data | Clinical Trial Data Analysis | Clinical trial | Data Analysis | Data Management | Data Visualization | Programming validation | Quality Control | R | Regulatory Standards | SAS | SAS Macro | SDTM
Education
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