Senior CRA: Medical Device, 50-75% Travel
Artivion, Inc.
Artivion, Inc. seeks a Site Monitoring & Management professional to independently oversee 10–15 investigational sites from start-up to close-out in Georgia. You will perform SIV/IMV/COV visits per the Monitoring Plan and ensure protocol/SOP/regulatory compliance (ISO 14155, FDA, local rules). You will conduct SDV/SDR, informed consent review, AE/SAE oversight, and maintain strong PI relationships. Travel 50–75% is required to support study execution. #J-18808-Ljbffr Artivion, Inc.
Vacancy posted 3 days ago
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