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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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to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Work Location Assignment: La Jolla, CA
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presentations as appropriate The ideal candidate possesses the following qualifications: Training and Education Extensive operational clinical trial experience A scientific or technical degree is preferred along
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