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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
  • Participates and fully assist in the overall management of the different program Offices within the Center for Biologics Evaluation and Research (CBER).
  • Recommends methods for improvement of office procedures and functions.
  • Assists in regularly communicating and sharing program information with other Program Offices and Center management officers and project mangers to ensure visibility and synergy of Office of the Director (OD) activities.
  • Keeps supervisory Management Officer aware of the status of projects managed including time frames and document requirements.
  • Participates in evaluations, management audits and similar reviews to identify recurring problems.

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