Clinical Research Associate

Hely: Budapest
Cég: BITRIAL Kft.
Kategória: Egészségügy, Gyógyszeripar

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 process University degree in health or naturaé science related fieldCRA experience is an advantageExcellent verbal and written communication skills in English and HungarianValid driving licenseDemonstrated flexibility in schedule and willingness to travel on a regular basisAbility to respond quickly to changing demands and opportunitiesDetail-oriented and efficient in time managementAdvanced skills and experience using Microsoft Office (Word, Excel, Power Point, Outlook)Knowledge of czech, slovak, polish, or romanian language is an advantage As a Clinical Research Associate you will have the unique opportunity to have an exciting career in the field of drug and medical device development as part of an expanding team.

Címkék: Employee status, University

profession.hu - 14 napja

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