Careers in Food and Drug Law

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Faegre Drinker Biddle & Reath LLP Logo
Faegre Drinker Biddle & Reath LLP

Washington, D.C.

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Food and Drug Administration (FDA) Logo
Food and Drug Administration (FDA)

Silver Spring, Maryland

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University of California Irvine (UCI)

Irvine, California

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University of Washington

Seattle, Washington

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Food and Drug Administration

Silver Spring, Maryland

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Cedars-Sinai Medical Center

Los Angeles, California

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Oregon Health and Science University

Beaverton, Oregon

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University of California Irvine (UCI)

Irvine, California

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Rutgers University

New Brunswick, New Jersey

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Cedars-Sinai Medical Center

Los Angeles, California

Food and Drug Administration (FDA) Logo
Food and Drug Administration (FDA)

Silver Spring, Maryland

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Veterans Affairs, Veterans Health Administration

Loma Linda, California

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California Department of Public Health

Sacramento, California

University of North Carolina at Chapel Hill

Chapel Hill , North Carolina

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University of Washington

Seattle, Washington

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University of Washington

Seattle, Washington

Albany College of Pharmacy and Health Sciences/Beigene/FDA Logo
Albany College of Pharmacy and Health Sciences/Beigene/FDA

Albany, New York

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University of California Irvine (UCI)

Irvine, California

Veterans Affairs, Veterans Health Administration Logo
Veterans Affairs, Veterans Health Administration

Loma Linda, California

Food and Drug Administration (FDA) Logo
Food and Drug Administration (FDA)

Silver Spring, Maryland

Food and Drug Administration (FDA) Logo
Food and Drug Administration (FDA)

Silver Spring, Maryland

University of California Irvine (UCI) Logo
University of California Irvine (UCI)

Irvine, California

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University of Washington

Seattle, Washington

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Regulatory Coordinator - Lymphoma
The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager and / 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 or


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