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    Duties

    Summary

    This position is located in the Center for Devices and Radiological Health, Office of Product Evaluation and Quality, Office of Clinical Evidence and Analysis, Division of Clinical Evidence and Analysis I which provides program/policy support for clinical evidence and regulatory oversight of medical devices to include biostatistical and epidemiologic analyses, development of data infrastructure, outreach and partnerships, and expertise on clinical investigations and real-world evidence.

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    Responsibilities

    • Develop public health policy and objectives, appraise programs, and initiate requirements for various post marketing epidemiological studies.
    • Evaluate data collection, perform data quality assessments, identify inadequacies and limitations of data and data utilization methods used to study epidemiological problems and issues.
    • Review and approve the substance of reports, decisions, case documents, contracts, or other action documents to ensure that policies accurately reflect the position at the organization and the views of the Agency.
    • Ensure that the organization's strategic plan, mission, vision, and values are communicated to the team and integrated into the team's strategies, goals, objectives, work plans and work products and services.

    Travel Required

    25% or less - You may be expected to travel for this position.

    Supervisory status

    No

    Promotion Potential

    None

  • Job family (Series)

    0601 General Health Science

This job originated on www.usajobs.gov. For the full announcement and to apply, visit www.usajobs.gov/GetJob/ViewDetails/597811000. Only resumes submitted according to the instructions on the job announcement listed at www.usajobs.gov will be considered.