Associate Principal Scientist, Statistical Programming
USA - New Jersey - Rahway, United States
USD 144K-224K Mid-level Full Time
Tasks
- Create SAS transport files and documentation
- Create tables and figures per modeling analysis plans
- Develop programming standards
- Develop statistical programming analysis reporting deliverables
- Ensure programmatic traceability from data source to modeling result
- Gather and interpret user requirements
- Integrate PK PD and covariate data for modeling ready datasets
- Lead data stewardship and modeling dataset creation
- Produce tables and graphics for study reports and regulatory submissions
- Programmatically synthesize preclinical and clinical data
- Represent statistical programming in process improvement activities
- Transform data into modeling ready analysis datasets
Perks/Benefits
- 401k
- Annual bonus
- Compassionate days
- Dental insurance
- Long-term incentive
- Medical insurance
- Other insurance benefits
- Paid Holidays
- Retirement benefits
- Sick days
- Vacation
- Vision insurance
Skills/Tech-stack
Clinical Trial Programming | Clinical endpoint data | Clinical trial | Data Filtering | Data Manipulation | Data Preprocessing | Data Step | Data Stewardship | Data traceability | Efficacy | Endpoint Data | Figures and Graphics | PK Parameters | Pharmacokinetic data | Project Management | R and D | R and D Programming | Regulatory Submissions | SAS | SAS Graph | SAS Macro | Safety | Table and Listing
Education
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