Statistical Programmer II
US - US - offsite, United States
R
USD 107K-138K Mid-level Full Time
Tasks
- Assess quality and consistency of analysis data
- Assist with study and systems audits
- Automate study deliverables using SAS macros
- Collaborate with clinical development to meet deliverables and timelines
- Contribute to continuous improvement of Programming Environment
- Generate statistical analysis datasets and outputs
- Participate in programming and clinical data science meetings
- Perform cross-study analyses
- Provide programming support based on analysis plan
- Provide programming support for study deliverables
- Review programming policies and SOPs
- Support electronic data submissions to regulatory agencies
Perks/Benefits
Skills/Tech-stack
CDISC ADaM | CDISC SDTM | Clinical trial | Clinical trial study design | Data submission | Electronic Data | Electronic data submission | ICH GCP | R | Regulatory Submissions | SAS | SAS Macros | Statistical Analysis | Study design
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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