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© All Rights Reserved. ApplyBlast.com
kymanox
The role supports US and EU regulatory submissions, including IND, NDA, BLA, 510(k), PMA, and related documentation, under the guidance of a Regulatory Strategy Lead. The specialist reviews technical and regulatory source documents, prepares briefing books, manages submission timelines, and interacts with regulatory authorities to ensure compliance and submission readiness.
Headquarters
Morrisville, North Carolina, United States
Company Size
201-500 employees
Founded
2004
Kymanox is a global life‑sciences services company that specializes in clinical trial supply chain management, offering packaging, labeling, storage, and distribution of investigational and comparator products. They operate temperature‑controlled depots and a worldwide logistics network to support study startup, inventory control, returns/destruction and regulatory‑compliant handling. Kymanox serves biopharma sponsors and CROs across phases with scalable, technology‑enabled supply solutions designed to maintain product integrity and ensure on‑time patient supply.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for kymanox.
kymanox didn’t post a salary, so this is our estimate from similar listings.
26% below the average for this role
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