Regeneron
Biotechnology
AssociateDirectorStatisticalProgramming-Pharmacometrics
Neural analysis suggests this role is
optimal for Director candidates.
“Associate Director Statistical Programming - Pharmacometrics at Regeneron. Skills: Statistical programming, Pharmacokinetics, Data analysis. Provide programming support. Lead programming support”
Industry & Context.
Data-driven analysis
4 days onsite
What They're Looking For.
Must Have
Master in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline, 10+ years of programming experience, Expert SAS programming skills, 4 days onsite presence
Nice to Have
Experience in project management, Experience in people management, Expertise in one or more therapeutic areas, SAS Certification desirable
What You'll Do.
Provide programming support
Lead programming support
Evaluate study requirements
Develop validation plan
Compile resource requirements
Identify changes in project requirements
Develop resource strategies
Lead programming and QC
Represent PMX programming functions
Coordinate activities
Create programming specifications
Manage programming specifications
Maintain programming specifications
Lead integration of data
Provide programming support
Plan creation of electronic submission requirements
Lead creation of electronic submission requirements
Plan validation of electronic submission requirements
Lead validation of electronic submission requirements
Provide timely support
Provide quality support
How You'll Work.
Team & Collaboration
Multidisciplinary study team; Cross line functions
Communication Scope
Communicate changes
Process & Methodology
Project management, Resource planning, Milestones
Full Job Description
**Associate Director Pharmacometrics Programming** provides timely support to the study team on all programming matters according to the project strategies. Provides project leadership, resource planning/coordinating deliverables within project or across multiple projects. Lead programming support for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, clinical pharmacology report requirement and programming specifications using internal standards and guidelines. Providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. The incumbent is responsible for addressing administrative functions required for project management such as compilation of resource requirements and milestones, identifying/communicating changes in project requirements that may affect key deliverables at the project level, and working with the department head to develop resource strategies. **_This position requires 4 days onsite presence based out of our Tarrytown, NY or Warren, NJ location._** **A typical day might include the following:** * Lead the programming and QC of analysis datasets, TFL's across multiple projects or standard tools following Regeneron standard data models or user requirements. Representation of PMX programming functions and coordination of activities with cross line functions and support planning/coordinating timelines in data exchange, deliverables. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. * Lead the integration of data across studies in support of Exposure-response, PopPK and PopPKPD analysis and 2.7.2. * Provide programming support for all PMX deliverable in HAR request, data dr
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