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Summary
A Sr. Manager provides support to the project team on programming matters within a therapeutic area, contributing to data processing from clinical studies, programming standards, and macro development. Responsible for leading programming deliverables, overseeing CROs, and supporting regulatory submissions.
Job Responsibilities
Coordinate and oversee programming, manage datasets, develop data models, mentor staff, and ensure quality standards are met for clinical trial data analysis and reporting.
Job Requirements
Masters Degree, 8-10 years experience, SAS certification desirable.
Salary Range
$148,300 - $241,900 annually.
Additional Information
Full-time, Mid-Senior level, in the field of Data/IT within the pharmaceutical/biotech industry. The job is active and accepting applications.