Teams at Enveda Biosciences

Lead global regulatory strategy for small molecules and combination products across development stages. Oversee interactions with FDA, EMA and other agencies; author and submit INDs, CTAs, briefing books, and response packages. Build and manage a high-performing regulatory team covering strategy, operations, and publishing to enable successful regulatory submissions and program advancement.

As a Senior Research Associate in In Vivo Pharmacology, you'll conduct efficacy studies, develop disease models, analyze data, and collaborate on innovative therapeutics.

Design, build, and maintain scalable data engineering infrastructure on Databricks and Azure. Implement CI/CD, IaC (Pulumi), monitoring, and automation. Collaborate with data scientists and platform teams, improve security and observability, mentor junior engineers, and maintain documentation and internal tooling.