# Associate Director, Global Regulatory Affairs at Kailera Therapeutics

- Company: Kailera Therapeutics
- What the company does: Kailera is a late clinical-stage biotechnology company advancing a diversified pipeline of GLP-1 therapies to provide options for people living with obesity. Backed by a16z.
- Company website: https://www.kailera.com
- Type: Startups
- Level: Principal and up
- Location: US-Remote
- Work setup: Remote
- Posted: 2026-09-18
- Apply by: 2026-11-02
- Apply: https://job-boards.greenhouse.io/kailera/jobs/5429240008
- Page: https://www.1752.vc/careers/jobs/kailera-therapeutics-associate-director-global-regulatory-affairs/

## About the role

The Associate Director, Global Regulatory Affairs will be responsible for day-to-day regulatory activities of early/late phase investigational products, leading the writing and submission of IND/CTA/amendments and future marketing application submissions, providing guidance to the team on regulatory filings and responses, and providing critical regulatory intelligence and guidance back to the team.

## What they're looking for

- Demonstrated knowledge of regulatory requirements in the design and conduct of clinical trials, including preparation of regulatory submissions
- Established working knowledge of regulatory guidelines and regulations (US and international)
- Demonstrated deep knowledge of the integrated drug development process
- Demonstrated ability to find solutions and alternatives through teamwork resulting in positive business outcomes
- Demonstrated ability to assess and manage risk in a highly regulated environment
- Strong written, spoken, and presentation communication

Tags: Regulatory