# Director, Regulatory Affairs at Arbor Software

- Company: Arbor Software
- What the company does: Who are we? Arbor Biotechnologies, a clinical stage, next-generation gene editing company based in Cambridge, MA, is advancing a portfolio of first-in-class genomic medicines addressing serious diseases for which there are no existing functional cures, with a... Backed by Accel.
- Company website: https://www.arbor.eco
- Type: Startups
- Level: Principal and up
- Location: Cambridge, MA
- Work setup: On-site
- Pay: $215K to $235K base salary per year (USD)
- Posted: 2026-08-25
- Apply by: 2026-10-12
- Apply: https://ats.rippling.com/arbor/jobs/21006716-b512-460b-be8d-54761945a22e
- Page: https://www.1752.vc/careers/jobs/arbor-software-director-regulatory-affairs/

## About the role

The Director of Regulatory Affairs is responsible for leading regulatory strategy and execution for Abror’s development programs across the portfolio, spanning preclinical and early clinical stages. Reporting to the Chief Medical Officer, this role serves as the Global Regulatory Lead on cross functional program teams and as the primary regulatory point of contact with FDA and other global health authorities.

## What they're looking for

- Bachelor’s degree in life sciences or related discipline required, advanced degree preferred
- Minimum of 10 years of experience in biotechnology or pharmaceutical development, including Regulatory Affairs experience
- Demonstrated experience leading or supporting regulatory strategy, submissions, and health authority interactions for preclinical and/or early clinical development programs
- Experience leading FDA interactions and/or IND submissions preferred
- Experience with biologics, gene therapy, or gene-editing products preferred
- Strong written and verbal communication skills, with the ability to synthesize complex scientific data into clear regulatory narratives

Tags: Development