Senior Scientist, Statistical Programming
$117,000–$184,200 year
On-siteRahway, New Jersey, United States
Job Summary
Support statistical programming activities for late-stage drug/vaccine clinical development projects by developing and executing analysis and reporting deliverables, including safety and efficacy datasets, tables, listings, and figures. Design and maintain statistical datasets for clinical development, outcomes research, and safety evaluation while collaborating with stakeholders to ensure timely project execution. Serve as the statistical programming point of contact throughout the product lifecycle, applying state-of-the-art methodologies to enable regulatory approval and global human health benefits. Lead one or more projects, ensuring compliance with CDISC and ADaM standards and leveraging SAS expertise for complex algorithm design and database optimization.
Required Qualifications
- Master's degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field
- 3 years experience in SAS programming in a clinical trial environment
- Bachelor's degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field
- 5 years experience in SAS programming in a clinical trial environment
- Experience in CDISC and ADaM standards
- Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH
- Systems and database expertise
- Ability to comprehend analysis plans which may describe methodology to be programmed
- Understanding of statistical terminology and concepts
- Strategic thinking ability to turn strategy into tactical activities
- Ability to design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices
- Ability to anticipate stakeholder requirements
- Familiarity with clinical data management concepts
- Knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)
- Must be a project leader and possess ability to complete tasks independently at a project level
- Ability to collaborate with key stakeholders
- Clinical Development
- Clinical Trials
- Computer Science
- Data Management
- Data Modeling
- Global Health
- Marketing
- Numerical Analysis
- Outcomes Research
- Project Leadership
- Stakeholder Engagement
- Stakeholder Relationship Management
- Statistical Analysis
- Statistical Programming
- Strategic Thinking
- Waterfall Model
- Working Independently
- Valid Driving License
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