Jobs at Korro Bio, Inc.

Support legal team with contract intake, review, administration, CLM maintenance, and corporate governance tasks including board materials, SEC filing support, equity administration, and due diligence. Maintain records, run reports, streamline processes, and assist with compliance and post-closing administration.

Lead analytical strategy for synthetic oligonucleotide drug substance and product: develop, transfer, qualify/validate analytical methods (LC-UV, LC-MS, HRMS, UV-Vis), manage CMO/CRO analytical activities, support stability and impurity characterization, author regulatory documentation, and lead investigations/OOS resolution to support clinical and regulatory progress.

Lead design, execution, and interpretation of GLP and non-GLP toxicology studies for oligonucleotide/RNA editing programs. Serve as toxicology SME on cross-functional teams, oversee external CRO studies (including international vendors), prepare regulatory safety documentation (IND/CTA/NDA/BLA), contribute to regulatory strategy and agency interactions, and mentor junior scientists.

Provide hands-on CMC quality oversight for CMOs and external vendors ensuring cGMP compliance across manufacturing, testing, batch release, audits, deviations/CAPAs, change control, and vendor qualification. Lead clinical lot disposition, audit programs, QTAs, inspection readiness, quality metrics, and support CMC regulatory submissions (INDs/IMPDs) for multi-regional clinical development.

Lead strategic and operational management of global clinical supply activities across development phases. Oversee supply planning, inventory, labeling, packaging, distribution, IRT/IXRS, vendor relationships, cold chain logistics, regulatory compliance, and QA collaboration to ensure timely, GMP-compliant delivery of investigational medicinal product to clinical sites worldwide.