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Korro Bio
60 First St, Cambridge, MA 02141
Source: Korro Bio careers · View original posting
From Korro Bio's posting. “We” and “our” refer to the employer.
Position Summary:: The Associate Director, Clinical QA will provide hands-on quality oversight of Korro Bio's clinical and nonclinical programs, ensuring that studies are conducted, and that data is generated and reported in compliance with Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Clinical Laboratory Practice (GCLP).
A central part of this role is planning and conducting audits of contract research organizations (CROs), laboratories, and other service providers, as well as audits of investigator sites, both in the US and internationally. This is an individual contributor role within a lean QA team, well suited to someone who enjoys a small-company environment and is equally comfortable leading an audit in the field and serving as the quality partner to study teams.
The role calls for sound, risk-based judgment and a practical approach to protecting patient safety, participant rights, and data integrity across Korro Bio's global clinical development programs.
Key Responsibilities:: Serve as the primary quality partner to Clinical Operations, Clinical Development, Regula-tory Affairs, Pharmacovigilance, Data Management, and Nonclinical teams, providing clear, practical guidance on GCP, GLP, and GCLP expectations throughout the study lifecycle.
Required Qualifications:: • Bachelor's degree in Life Sciences or related scientific discipline required.
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