CVRx, Inc. is seeking a Clinical Research Associate III (CRAIII) to manage day-to-day operations of clinical trials and monitor sites to ensure compliance with study protocols, SOPs, CVRx requirements, GCP, and regulatory rules. The role may work from a CVRx office or at sites as monitoring occurs.
This position involves traveling up to 40% within the US and coordinating with Clinical Project Managers, Data Management, Safety, Regulatory, and QA teams to ensure end-to-end study execution.
#J-18808-LjbffrRemote CRA III Clinical Trials Monitor & Site Liaison in workfromhome at Unknown Company
This position is listed as full time and onsite.