Clinical Trials Regulatory & Data Coordinator; Hybrid
Listed on 2026-10-07
-
Research/Development
Clinical Research
ERA Health Research in Redmond, WA seeks a Full-Time Regulatory and Data Coordinator I to support study activation, regulatory document management, and data quality. Hybrid work model with on-site training initially. Responsibilities include IRB submissions, EDC data entry, regulator binder maintenance, and monitoring preparation.
The role requires a Bachelor’s degree in a related field and 1–2 years of regulatory support experience, plus strong attention to detail and communication skills.
This posting is for the Clinical Trials Regulatory & Data Coordinator (Hybrid) role at Eastside Research Associates, based in Redmond, WA, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Trials Regulatory & Data Coordinator (Hybrid) role in the description above.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).