Clinical Research Associate

Feladatok: Conduct different types of monitoring visits (pre-study visits, site initiation visits, interim monitoring visits & close out visits)Develop and maintain site and investigator relationships to ensure clinical trials are managed efficientlyPerform source document verification and prepare monitoring visit reports, including confirmation and follow-up letterManage the study documentation and other essential trial related documentsSupport regulatory submissions to the Competent AuthorityParticipate in Investigator selection/feasibility processEgészségügyi szakember; Klinikai kutató

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