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Associate Director, Clinical QA — GCP Compliance & Audits

Job in San Diego, San Diego County, California, 92189, USA
Listing for: ADARx Pharmaceuticals, Inc.
Full Time position
Listed on 2026-10-06
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
  • Pharmaceutical
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 175000 - 195000 USD Yearly USD 175000.00 195000.00 YEAR
Job Description & How to Apply Below

ADARx Pharmaceuticals, Inc. is seeking an Associate Director of Clinical Quality Assurance to lead GCP compliance across all clinical programs. You will build a risk-based quality framework and partner with cross-functional teams to ensure readiness for regulatory submissions and inspections.

You will oversee audits of CROs and vendors, review INDs and NDA-related materials, and drive CAPA and training programs to embed quality throughout development.

We would love to welcome a new Associate Director, Clinical QA — GCP Compliance & Audits to our group in San Diego, CA, United States.

The Associate Director, Clinical QA — GCP Compliance & Audits role at ADARx Pharmaceuticals, Inc. is now open for applications in San Diego, CA, United States.

Join us at ADARx Pharmaceuticals, Inc. as our next Associate Director, Clinical QA — GCP Compliance & Audits in San Diego, CA, United States.

Position Requirements
10+ Years work experience
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