About this role
Role Overview
- Provide timely support to the study team on all programming matters according to the project strategies
- Develop an expertise within a therapeutic area or standard tool
- Work with minimal supervision to perform, coordinate and oversee the preparation, execution, reporting and documentation of a project
- Function as a lead programmer in the development and QC of tables, listings, graphs, or systems in support of analysis requirements utilizing Regeneron tools and methodologies and current industry standards (i.e. CDISC SDTM / ADaM)
- Manage the effort, including esubmission deliverables
- Provide programming support for complex presentations and more complex statistical ad-hoc requests
- Act as programming representative in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports
- Review and select resumes, screen and interview candidates for contractor and permanent positions
- Provide feedback to management regarding team member’s contributions to the work effort for evaluating individual's performance and recommend yearly goals
Requirements
- Master’s Degree
- 8-10 years of relevant work experience
- SAS Certification desirable
- 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry
- some project and people management experience with a Master’s Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline
Benefits
- health and wellness programs (including medical, dental, vision, life, and disability insurance)
- fitness centers
- 401(k) company match
- family support benefits
- equity awards
- annual bonuses
- paid time off
- paid leaves (e.g., military and parental leave) for eligible employees at all levels