Supports the Defense Health Agency Force Health Protection division with oversight of product management and clinical protocol accountability. Manages Investigational New Drug (IND) products, ensures Good Clinical Practice compliance, delivers GCP training, and coordinates with FDA and IRBs on submissions. Contingent upon contract award.
Requirements
Bachelor’s in a scientific/health field; 8+ years clinical/FDA regulatory product development; cGCP/cGLP/cGMP knowledge. Clearance per posting: ability to obtain NACI (background investigation, not a security clearance).
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