Responsibilities
The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, “Ich o bună practică clinică: Ghid consolidat,” (GCPS), Sprijinirea programelor client administrate de Whatermark Asigurați -vă că datele proiectului și declarațiile sumare sunt de calitate cunoscută și documentată.
Requirements
Will be expected to travel extensively to study sites in the US to monitor our clinical and outcome studies.
Successful applicant must have previous experience monitoring clinical trials.
Basic knowledge of worldwide regulatory requirements and/or pharmaceutical development practices.
Knowledge/understanding of the approach and perspectives of regulatory agencies.
Essential Skills and Abilities
Good written and verbal communication skills, demonstrated ability to function effectively with all levels of management
Strong negotiation and relationship building skills
Good understanding of medical / corporate governance principles
Detailed oriented and organized
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