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CLINICAL TRIAL ASSOCIATE-DOCUMENT MANAGEMENT SPECIALIST

Assists with the development of critical study related documents, including but not limited to, clinical protocols, Informed Consent Forms (ICFs), operational documents, study reference documents, study newsletters, site materials...

CompanyAdc Therapeutics
AddressNew Providence, NJ
CategoryHuman Resources
Job typeFull-Time
Date Posted a month ago See detail

Clinical Trial Associate-Document Management Specialist

Adc Therapeutics

New Providence, NJ

Assists with the development of critical study related documents, including but not limited to, clinical protocols, Informed Consent Forms (ICFs), operational documents, study reference documents, study newsletters, site materials...

a month ago seen See more...

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