DMPK Study Coordinator – Cross-Functional Biotech
Listed on 2026-10-11
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Healthcare
Clinical Research -
Research/Development
Clinical Research, Research Scientist
Editas Medicine, a leader in genome editing, seeks a Study Coordinator to support nonclinical drug development at Cambridge, MA. You will manage timelines, documents, and sample logistics within the DMPK, Nonclinical Safety, and Translational Science teams.
You will coordinate data, ensure LIMS integrity, and partner with science and informatics to streamline workflows. This six-month contractor role offers exposure to multiple stages of drug development.
This is an excellent position to take on the DMPK Study Coordinator – Cross-Functional Biotech Role role at Editas.
The DMPK Study Coordinator – Cross-Functional Biotech Role role at Editas is now open for applications in Cambridge, MA, United States.
Join us at Editas as our next DMPK Study Coordinator – Cross-Functional Biotech Role in Cambridge, MA, United States.
We are currently recruiting a DMPK Study Coordinator – Cross-Functional Biotech Role for our team in Cambridge, MA, United States.
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