Description
Pathos is seeking a highly experienced individual to manage the entire IND lifecycle for their oncology pipeline. This role involves authoring DSURs, preparing IB updates and IND amendments, building FDA meeting packages, managing ClinicalTrials.gov listings, and overseeing eCTD publishing. The successful candidate will be responsible for directing AI agents to handle regulatory tasks, applying expert judgment to review and finalize outputs, and collaborating with engineering teams to enhance AI capabilities. This hybrid role requires up to three days per week in New York City.
