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About Center
The Center for Biologics Evaluation and Research (CBER) uses sound science and regulatory expertise to:
Protect and improve public and individual health in the United States and, where feasible, globally; Facilitate the development, approval of, and access to safe and effective biological products and promising new technologies; and Strengthen CBER as a preeminent regulatory organization for biological products.

Responsibilities
  • Evaluates and Analyzes Clinical Trial Data.
  • Prepares authoritative reports and recommendations related to clinical trials of consideration breadth and diversity.
  • Serves as a Microbiologist and senior researcher in the conduct and leadership of the research activities of the laboratory.
  • Carries out experimental procedures, collects data, and takes full responsibility for all phases of the project, including interpretation of findings.
  • Determines whether the concepts, theories, and practices developed by others can be utilized in the regulatory area.
  • Serves as Technical expert on controversial issues on the evaluations, interpretations, and recommendations of the data in final form for publication.

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