Recursion

Oversee all clinical aspects of early-phase trials, including authoring protocols, medical monitoring, and managing site interactions. Responsible for ensuring study data quality and collaborating cross-functionally to advance drugs from IND through proof of concept.

Lead the development and implementation of global regulatory strategies for assigned drug discovery programs across multiple jurisdictions. Collaborate with cross-functional teams to manage regulatory risks and oversee the submission of critical documentation to health authorities.

Interns will have the opportunity to contribute to impactful work that changes lives. They will be part of a team that values integrity, collaboration, and innovation.