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documents such as Pre-INDs, INDs, BLAs, and IMPDs. Collaborate with regulatory partners to prepare Orphan Drug Designation (ODD) requests based on pre-clinical efficacy data and disease prevalence, submitting
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the facility is in a clean, organized, and professional appearance. Areas include bio-hazard, quarantine, and rodent immunocompetent and immunodeficient areas. Train new hires on CCM policies and procedures and
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