Your primary responsibility will be validating and quality checking safety database fields on assigned projects.
You will also provide input for and review relevant safety tracking systems for accuracy/quality and perform safety review of clinical data (case report forms) and patient labs.
You will also be responsible for documenting and processing serious adverse event cases within ICON, regulatory authorities and sponsor regulations and timeframes
Get Placement Papers here to prepare for writtent test and interview
Get Sample Resumes here
Get Technical Material & Interview Tips here
Like and let your friends know about this on facebook