Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) - Early Phase
GBR-Remote, United Kingdom
R
GBP 53K-91K (estimate) Senior-level Full Time
Tasks
- Attend regulatory agency meetings
- Coach and mentor biostatistics staff
- Conduct verification and quality control of deliverables
- Coordinate biostatistics and statistical programming activities
- Create or review programming specifications
- Develop mock up displays for tables listings and figures
- Ensure outputs match SAP and specifications
- Follow SOPs and regulatory guidelines
- Generate randomization schedules
- Input to clinical study reports
- Lead integrated analysis projects
- Maintain project documentation and QC documents
- Manage scheduling across multiple projects
- Monitor study progress against milestones
- Participate in data monitoring committee activities
- Participate in data safety monitoring board
- Perform independent review of statistical work
- Prepare statistical analysis plans
- Provide statistical programming support
- Review SAS annotated case report forms
- Review database design and study documentation
- Serve as biostatistics representative on project teams
- Support business development proposals and budgets
- Support statistical tasks across project lifecycle
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | Biostatistics | Clinical study | Clinical study report | Clinical trials | Data Monitoring | Data Monitoring Committee | Data Safety | Data Safety Monitoring Board | Data safety monitoring | ICH | Integrated Analysis | Quality Assurance | Quality Control | Randomization | SAS | SAS programming | Statistical Analysis | Statistical Analysis Plan | Statistical programming
Education
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