Senior Statistical Programmer I/II (CVRM)
Tasks
- Apply project management practices to programming aspects
- Collaborate with statisticians lead programmer data managers and study leaders
- Contribute to develop best practices for programming quality and efficiency
- Coordinate with contract programming providers
- Deliver clinical programming work with quality and timeliness
- Ensure compliance to standards and automation usage
- Ensure quality of own deliverables and other programmers deliverables
- Identify manage and communicate risks for clinical studies
- Implement statistical programming aspects of protocol
- Lead technical initiatives
- Plan and lead programming team activities and tasks
- Program independently with efficiency and quality
- Provide programming subject matter expertise to stakeholders
- Write specifications and oversee documentation completeness
Perks/Benefits
Skills/Tech-stack
CDISC | Clinical Development | R | SAS | SAS Macro
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
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