Kelsey Bludorn

Director Of Research Operations at DaVita Clinical Research

Kelsey Bludorn has extensive experience in project management and regulatory affairs, currently serving as a Senior Manager of Project Management at DaVita Clinical Research since September 2012. Responsibilities include managing site start-up activities, maintaining communication with sponsors and various stakeholders, and overseeing regulatory document quality control. Prior to this role, Kelsey was a Regulatory Affairs Manager at Sioux Falls VA Health Care System, where professional skills were developed as an intern in the Public Affairs Department. Kelsey earned a Bachelor of Business Administration in Health Care Administration from the University of South Dakota.

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Minneapolis, United States

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DaVita Clinical Research

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DaVita Clinical Research (DCR) is the bridge linking DaVita services to the pharmaceutical and biotech research community. DCR provides comprehensive multi-specialty (Phase II-III) clinical trial services to the pharmaceutical and biotech industry. Since our founding, our organization has conducted more than 500 clinical trials with more than 175 pharmaceutical companies. At DCR, we help scientists and doctors. We think helping to cure people seems like a good goal to have. But we need your help, too.