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Administracja biurowa » Pracownik biurowy

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CTA Belgium Nr ref.: /JOBS.pl We are looking for a Clinical Trial Associate to work for our client a small Biotech company located in Belgium. This organization develops drugs based on human antibodies for orphan / rare diseases (oncology and immunology). Duties & Responsibilities Be accountable for providing logistical support for a clinical program and associated clinical trials Be accountable for delivery of complete Trial Master File (TMF) for assigned studies or program Be responsible for the collection, review and tracking of regulatory documents for assigned clinical studies Be responsible for the timely and accurate input of study-related information into Impact Be responsible for preparation and distribution of regulatory and operational binders/manuals and clinical system set-up Be responsible for processing clinical grant payments to investigative sites and clinical trial material requests Provide oversight and quality assessment of document standards, tools and processes at the program level Act as a primary logistical point of contact with investigative sites Requirements BA/BS/BSN degree is required At least 3 years previous experience in the healthcare field; pharma experience strongly preferred; with a basic understanding of drug development and knowledge of ICH and GCP guidelines is desired Must have good interpersonal, written and verbal communication skills and strong computer skills Fluent in English Should be a team player capable of working in a multi-cultural environment Only candidates living in Belgium are invited to apply. Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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