• Help

    Duties

    Summary

    This position is located in the Department of Health and Human Services, Food and Drug Administration, Office of Medical Products and Tobacco, Center for Drug Evaluation and Research, Office of Translational Sciences, Office of Computational Science in Silver Spring, MD.

    This vacancy is also being announced concurrently with vacancy announcement FDA-CDER-18-MP-10226486 under merit promotion procedures. Applicants must apply separate for each announcement in order to be considered under both.

    Learn more about this agency

    Responsibilities

    • Provide oversight and guidance to personnel in the Center and regulated industry on data management tools
    • Analysis of regulatory review information/data needs in relation to existing capabilities for providing information to management on a variety of topics associated with the review process.
    • Responsible for the overall integrity and accuracy of information and data tools in the automated system, providing on site and local training, consultation for electronic submission.
    • Responsible for coordinating and/or providing both periodic and special reports pertaining to product review status and other matters related to various regulatory review activities for product and establishment submission handle by the Center.
    • Provide on-site and classroom based training to scientific reviewers, project management staff, administrative personnel, and managers on how to use internal systems, desktop productivity tools, and data analysis tools.

    Travel Required

    Not required

    Supervisory status

    No

    Promotion Potential

    13

This job originated on www.usajobs.gov. For the full announcement and to apply, visit www.usajobs.gov/GetJob/ViewDetails/506204600. Only resumes submitted according to the instructions on the job announcement listed at www.usajobs.gov will be considered.