Associate Principal Scientist, Statistical Programming
USA - Pennsylvania - North Wales (Upper Gwynedd), United States
R
USD 142K-224K Mid-level Full Time
Tasks
- Create SAS transport files and documentation for regulatory submissions
- Develop programming standards for production quality
- Develop tables and figures according to analysis plans
- Ensure data source to modeling result traceability
- Gather and interpret user requirements
- Integrate PK PD and covariates into modeling ready datasets
- Lead data stewardship for modeling datasets
- Provide statistical programming analysis and reporting deliverables
- Represent statistical programming in process improvement
- Retrieve and transform data into modeling ready datasets
- Synthesize preclinical and clinical data into analysis structures
Perks/Benefits
- 401k
- Annual bonus
- Compassionate days
- Dental insurance
- Long-term incentive
- Medical insurance
- Paid Holidays
- Sick days
- Vacation
- Vision insurance
Skills/Tech-stack
Clinical Trial Programming | Clinical data | Clinical data management | Clinical trial | Data Management | Data Preprocessing | Data Step | Data Transformation | Data Validation | Graph generation | Listings Generation | PD analysis | PK modeling | Pharmacokinetics | SAS | SAS Graph | SAS Macro | Statistical programming | Table Generation
Education
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