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Abbott

Pittsburgh, Pennsylvania

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U.S Food and Drug Administration, Center for Devices and Radiological Health Logo
U.S Food and Drug Administration, Center for Devices and Radiological Health

Silver Spring, Maryland

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Stanford University

Stanford, California

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University of Southern California (USC)

Los Angeles, California

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Cedars-Sinai Medical Center

Los Angeles, California

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Abbott

Austin, Texas

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Abbott

St. Paul, Minnesota

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University of Southern California (USC)

Los Angeles, California

FDA - Center for Devices and Radiological Health (CDRH) Logo
FDA - Center for Devices and Radiological Health (CDRH)

Silver Spring, Maryland

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University of Washington

Seattle, Washington

FDA Center for Devices And Radiological Health (CDRH)

Silver Spring, Maryland

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Kelly Science & Clinical

Rockville, Maryland

FDA - Center for Devices and Radiological Health (CDRH) Logo
FDA - Center for Devices and Radiological Health (CDRH)

Silver Spring, Maryland

FDA - Center for Devices and Radiological Health (CDRH) Logo
FDA - Center for Devices and Radiological Health (CDRH)

Silver Spring, Maryland

U.S Food and Drug Administration, Center for Devices and Radiological Health Logo
U.S Food and Drug Administration, Center for Devices and Radiological Health

Silver Spring, Maryland

U.S Food and Drug Administration, Center for Devices and Radiological Health Logo
U.S Food and Drug Administration, Center for Devices and Radiological Health

Silver Spring, Maryland

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University of Washington

Seattle, Washington

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University of Washington

Seattle, Washington

U.S Food and Drug Administration, Center for Devices and Radiological Health

Silver Spring, Maryland

FDA Center for Devices And Radiological Health (CDRH)

Silver Spring, Maryland

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Abbott

MapleGrove, Minnesota

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University of Health Sciences and Pharmacy in St. Louis

St. Louis, Missouri

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Regulatory Coordinator II - Clinical Trials Office
The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on assigned studies to ensure regulatory compliance with DFCI and DF/HCC policies as well as federal regulation and ICH/GCP guidelines. This position will work collaboratively with a variety of personnel at all levels, including faculty and study team members of DF/HCC and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizatio


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