Regeneron

ManagerStatisticalProgramming

$129–210k Cambridge, Massachusetts, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“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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