Обязанности и достижения:
To support the clinical research teams with ongoing conduct of studies;
To assist project teams with study specific documentations as appropriate:
- preparing study-specific procedures, drug accountability records,
completion of status reports, proof reading newsletters and merge letters etc.
To coordinate the document translation;
To assist in the preparations, handling and tracking of Ethics/Regulatory submissions;
To assist in coordination of Investigator payments;
To maintain the study files for the project;
To assist project teams with trial progress tracking by updating the Clinical Trial Management System;
To organize project team meetings and take minutes, as required;
To coordinate document ordering/dispatch of trial materials
e.g. Case Report Forms, diary cards, lab supplies as appropriate.