# Director, Regulatory Affairs at Eikon Therapeutics

- Company: Eikon Therapeutics
- What the company does: Advancing breakthrough therapeutics through the purposeful integration of science and engineering. Backed by Lux.
- Company website: https://eikontx.com
- Type: Startups
- Level: Principal and up
- Location: Jersey City, NJ
- Work setup: On-site
- Pay: $213K to $257K base salary per year (USD)
- Posted: 2026-05-29
- Apply by: 2026-10-08
- Apply: https://job-boards.greenhouse.io/eikontherapeutics/jobs/5150121007
- Page: https://www.1752.vc/careers/jobs/eikon-therapeutics-director-regulatory-affairs/

## About the role

We are seeking an experienced Director, Regulatory Affairs to support and execute regulatory strategy across our clinical-stage development programs. In this role, you will play a key role in both shaping regulatory strategy and driving hands-on execution across assigned programs.

## What they're looking for

- Regulatory Strategy: Contribute to the development and execution of regulatory strategies supporting product development, approval, and commercialization in alignment with company objectives
- Regulatory Compliance: Maintain current knowledge of evolving regulations, guidance, and industry best practices to ensure ongoing compliance across programs
- Submission Management: Lead and/or support the preparation, review, and submission of regulatory documents, including INDs, NDAs, and MAAs, as applicable
- Cross-Functional Collaboration: Work closely with Clinical Development, R&D, Quality, and other stakeholders to integrate regulatory considerations throughout the development lifecycle and drive alignment
- Quality Support: Support regulatory aspects of quality systems, including compliance with GCP and GLP requirements
- Risk Assessment: Identify regulatory risks, assess potential impact, and proactively recommend mitigation strategies

Tags: Clinical Regulatory