Regeneron
ManagerStatisticalProgramming
Neural analysis suggests this role is
optimal for Manager candidates.
“Manager Statistical Programming at Regeneron. Skills: Statistical programming, Clinical trials, Project management. Provide study team support. Provide project leadership”
What They're Looking For.
Must Have
Master's Degree, 8-10 years relevant work experience, 5+ years programming experience, project management experience, people management experience
Nice to Have
SAS Certification desirable
What You'll Do.
Provide study team support
Provide project leadership
Provide programming support
Identify requirements
Implement programming standards
Execute programming standards
Lead programming aspect
Oversee documentation
Ensure code maintenance
Ensure log maintenance
Ensure output maintenance
Perform project tasks
Coordinate project tasks
Oversee project tasks
Prepare project documentation
Execute project documentation
Report project documentation
Allocate work required
Summarize work required
Provide ad hoc support
Act as programming representative
Ensure timely support
Ensure quality support
Lead application development
Determine resource requirements
Recommend yearly goals
Advise direct reports
Advise on data retention
Advise on records retention
Advise on information retention
How You'll Work.
Team & Collaboration
Study team; Multidisciplinary team; User audience
Process & Methodology
Project management
Full Job Description
_***Please note this is an onsite role and NOT eligible remote._ A Manager provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study team, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan, programming specification or user requirements document using internal standards and guidelines. The incumbent provides guidance in implementing and executing the programming and project standards. The incumbent will be responsible for leading the programming aspect of a project, both internally or CROs, for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards and annual reports. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. Meets statistical ad hoc requests of senior management. **A typical day in this role looks like:** * 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 esubmssion deliverables, using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming 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
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