# Senior Director, 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: 2026-09-22
- Apply by: 2026-11-06
- Apply: https://jobs.lever.co/artbio/ce060b5c-b7d0-4806-a335-497f12061754?utm_source=1752vc&utm_medium=careers
- Page: https://www.1752.vc/careers/jobs/artbio-senior-director-regulatory-affairs/

## About the role

The Senior Director, Regulatory Affairs leads and coordinates regulatory interactions and submission execution for ARTBIO’s clinical-stage radiopharmaceutical programs. This role is primarily responsible for coordinating regulatory medical writing across functions. The position works cross-functionally to translate research and development data and strategy into clear, compliant regulatory communications and high-quality submission deliverables. Found on 1752vc Careers, the job board for startup and VC roles.

## What they're looking for

- Bachelor’s degree in a scientific, medical, pharmacy, or related discipline is required, an advanced degree is preferred
- Strong knowledge of US FDA requirements and interaction processes
- Proven track record coordinating US INDs, IND amendments, annual reports, health authority meeting packages, and responses to US FDA information requests
- Hands-on experience with electronic submission publishing, document management, submission standards, and external publishing vendors
- Experience and familiarity with leading submission of New Drug Applications, Marketing Authorization Applications, and radiopharmaceutical development are helpful

Tags: Regulatory

Source: 1752vc Careers, https://www.1752.vc/careers/jobs/artbio-senior-director-regulatory-affairs/