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Associate Director, Clinical QA at Korro Bio - ApplyBlast

Associate Director, Clinical QA

Korro Bio

22 days ago

Cambridge, Massachusetts, United States

Hybrid

Full Time

Director

0 applicants

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About this role

The Associate Director, Clinical QA provides hands-on quality oversight for Korro Bio's clinical and nonclinical programs, ensuring compliance with GCP, GLP, and GCLP standards. This individual contributor role involves planning and conducting audits of CROs, laboratories, and investigator sites while serving as a quality partner to study teams. The position requires risk-based judgment to protect patient safety, participant rights, and data integrity across global clinical development programs.

Responsibilities

Plan and conduct audits of CROs, laboratories, and investigator sites
Manage clinical and nonclinical quality events including deviations and CAPAs
Provide quality oversight and guidance on GCP, GLP, and GCLP compliance

Skills

Qualifications

Bachelor's degree in Life Sciences or related scientific discipline

About Korro Bio

korrobio.com

Headquarters

Cambridge, Massachusetts, United States

Company Size

51-200 employees

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Korro Bio is a biotechnology company developing precision RNA‑editing therapeutics that edit a single letter on RNA to modulate biological pathways. Their mission is to translate this platform into genetic-medicine solutions for complex, prevalent diseases by advancing a focused therapeutic pipeline. The company emphasizes moving its science toward patient‑facing programs and resources (for example, work relevant to AATD) to deliver targeted, durable treatments.