Clinical Study Manager
Posted on Mar 17, 2019 by Hobson Prior
Assurance of upholding project timelines, quality standards and study objectives.
Preparation and clearance of study documents with CROs as well as the selection of contract partners
Compilation of documents for the authorization of clinical studies, for ethics commissions and for federal authorities
Planning and conduct of training sessions relevant to the studies as well as team and investigator meetings
Preparation of study information according to regulatory requirements
Degree in natural sciences or completed medical vocational training
Professional experience as a Clinical Study Manager, CRA/Clinical Monitor (m/f) or in a similar function
Profound knowledge in the field of oncological studies. Very good knowledge of relevant laws and regulations (e.g. ICH GCP guideline)
Proactive, independent way of working as well as excellent communication and organization skills
Professional handling of MS Office
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