# Head of Regulatory Affairs at ARTBIO

- Company: ARTBIO
- What the company does: Learn about how ARTBIO is redefining cancer care through a new class of alpha radioligand therapies and building an ecosystem to maximize their potential. Backed by Third Rock Ventures.
- Company website: https://artbio.com
- Type: Startups
- Level: Principal and up
- Location: Cambridge, MA
- Work setup: Remote
- Posted: 2026-09-08
- Apply by: 2026-10-23
- Apply: https://jobs.lever.co/artbio/dc0fdf83-d9a7-4dd6-84f4-3407cf0159b1
- Page: https://www.1752.vc/careers/jobs/artbio-head-of-regulatory-affairs/

## About the role

The Head of Regulatory Affairs leads ARTBIO’s regulatory function for clinical-stage radiopharmaceutical programs, ensuring clear strategy, compliant execution, and effective engagement with health authorities. This is a key leadership position that requires a deep understanding of regulatory processes and a proven track record of successfully navigating regulatory landscapes in the biotech or pharmaceutical industry.

## What they're looking for

- Advanced degree (JD, PhD, PharmD, MD or equivalent) in a scientific discipline is preferred
- 15+ years of regulatory affairs experience in the biotech or pharmaceutical industries, with emphasis on drug development
- Possess in-depth knowledge of global regulatory requirements and guidelines, including FDA, and EMA regulations and international regulatory frameworks
- Proven track record of successful regulatory submissions, including INDs, NDAs, BLAs and MAAs
- Experience leading regulatory affairs strategies for complex programs across multiple therapeutic areas
- Strong understanding of drug development processes, CMC, quality, and clinical trial regulations

Tags: Regulatory