Manager Statistical Programming providing timely support for clinical studies and project leadership at Regeneron. Overseeing programming and documentation for data processing from clinical studies.
Responsibilities
Provides timely support to the study team on all programming matters according to the project strategies
Provides project leadership and programming support for processing data from clinical studies
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
Manage the effort, including esubmission 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 reports
If applicable, lead an application development and act as the programming representative to the user audience
Review and select resumes, screen and interview candidates for contractor and permanent positions
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)
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