Principal Statistical Programming Consultant (EU)
Tasks
- Collaborate to resolve data issues
- Create SAS programs for graphs and tables
- Develop SAS analysis datasets
- Execute data migration from legacy datasets
- Follow SOP and quality management systems
- Implement CDISC standards
- Lead study team
- Mentor programmers
- Perform data validation and transformation
- Perform statistical programming for clinical trials
- Process clinical study report deliverables
- Read and implement program specification documents
- Support hiring by defining skills and conducting interviews
- Validate SAS tables listings figures
Perks/Benefits
- Career growth
- Collaborative work environment
- Global clinical trials experience
- Leadership opportunities
Skills/Tech-stack
ADaM | CDISC | Clinical Trial Data | Clinical trial | Data Migration | Data Transformation | Data Validation | Drug development | Management systems | Quality Management Systems | Quality management | Regulatory Submissions | SAS | SDTM | TLF generation | Trial data
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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