The Director of Regulatory Affairs will lead global regulatory strategy and oversee regulatory processes for assigned programs. They will collaborate with cross-functional teams to ensure successful registration and lifecycle management of products across various jurisdictions.
You will lead the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, including designing clinical studies and managing regulatory interactions. Additionally, you will collaborate with cross-functional teams to solve drug development challenges using modeling and simulation.
You will lead the clinical pharmacology and pharmacometrics strategy for oncology and rare disease programs, including designing clinical studies and managing regulatory interactions. Additionally, you will collaborate with cross-functional teams to solve drug development challenges using modeling and simulation.
Lead a team in building and optimizing the machine learning infrastructure that powers a drug discovery platform. You will collaborate cross-functionally to enable the scaling of AI/ML, LLM, and agentic systems across supercomputing and cloud environments.
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.
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.
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.
