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    Duties

    Summary

    This position is located in the Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, Office of Generic Drugs, Office of Bioequivalence, Division of Bioequivalence I, located in Silver Spring, Maryland.

    Learn more about this agency

    Responsibilities

    • Reviews and evaluates study data and test results submitted in drug products applications, and makes regulatory decisions on the acceptability of the study and approvability of the applications.
    • Extends and modifies approaches, precedents and methods to solve a variety of pharmacokinetic and pharmacology problems with unprecedented and obscure aspects.
    • Provides leadership, guidance and regulatory expertise to address and solve complex regulatory issues consistent with technological developments or new scientific evidence and provides innovative solutions to complex problems.
    • Serves as the program resource for information on current concepts in pharmacokinetics and pharmacology.

    Travel Required

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

    Supervisory status

    No

    Promotion Potential

    None

  • Job family (Series)

    0405 Pharmacology

This job originated on www.usajobs.gov. For the full announcement and to apply, visit www.usajobs.gov/GetJob/ViewDetails/512302600. Only resumes submitted according to the instructions on the job announcement listed at www.usajobs.gov will be considered.