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Senior Director, Regulatory Affairs

Job in San Jose, Santa Clara County, California, 95199, USA
Listing for: Proclinical Staffing
Full Time position
Listed on 2026-07-17
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 140000 - 180000 USD Yearly USD 140000.00 180000.00 YEAR
Job Description & How to Apply Below
Position: (Senior) Director, Regulatory Affairs

Director, Regulatory Affairs – Permanent – Remote

Proclinical is seeking a (Senior) Director, Regulatory Affairs for an exciting MASH‑focused biotechnology company based in California.

Primary Responsibilities:

In this role, you will lead U.S. regulatory strategy for their lead product and future liver fibrosis programs. This role will lead FDA engagement and regulatory data positioning, while overseeing regulatory submission mechanics executed by external service providers, with a particular focus on leveraging foreign clinical data to support U.S. regulatory pathways. The position is based remotely within the United States.

Skills & Requirements:

  • 8–12+ years of regulatory affairs experience in the biopharmaceutical industry.
  • Demonstrated experience leading IND submissions and FDA interactions.
  • Experience supporting Phase 2 and/or Phase 3 clinical programs.
  • Direct experience leveraging foreign (ex‑U.S.) clinical data in FDA discussions.
  • Advanced scientific degree (PhD, PharmD, MD, MS) or equivalent experience.
  • Recent experience in liver disease, fibrosis, MASH/NASH, or chronic hepatitis.
  • Familiarity with FDA guidance on fibrosis endpoints and non‑invasive biomarkers.
  • Experience working across U.S., EU, and China regulatory environments.

The (Senior) Director, Regulatory Affairs will:

  • Develop and execute U.S. and potentially global regulatory strategies supporting Phase 2 (MASH) and Phase 3 (CHB) clinical programs.
  • Lead FDA interactions including Pre‑IND, IND, Type B, and Type C meetings.
  • Own regulatory positioning for the use of foreign clinical data in U.S. development discussions.
  • Manage external regulatory service providers responsible for IND publishing and submission logistics.
  • Review, author, and critically edit regulatory documents including IND modules, briefing books, clinical protocols, and agency responses.
  • Partner closely with Clinical Development to ensure regulatory‑aligned protocol design and endpoint selection.

For questions or to apply, please contact Phu Huynh at +1 646‑779‑7961 or

Proclinical Staffing is an equal opportunity employer. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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Position Requirements
10+ Years work experience
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