Regeneron

Biotechnology

AssociateDirectorStatisticalProgramming-Pharmacometrics

$176–287k Tarrytown, New York, United States; Warren, New Jersey, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Director candidates.

The Brief

“Associate Director Statistical Programming - Pharmacometrics at Regeneron. Skills: Statistical programming, Pharmacokinetics, Data analysis. Provide programming support. Lead programming support”

Industry & Context.

Biotechnology
Problems you'll solve

Data-driven analysis

Eligibility Requirements

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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