I am employee working in pharmacovigilance, but I have always been drawn to and still am interested in trying another part of this medical field, namely regulatory affairs, for an even greater understanding of the area, especially since I always enjoy learning new things.
- editing, scanning, printing and filling of the documents according to good documentation practice and company quality system
- supporting reports and RFI questionnaires compilation
- monitoring of Company/project specific Safety mailboxes and tracking
- administrative support in communication with internal and external vendors
- support of all staff in the Global Drug Safety department in running projects or processes
- support in projects compliance monitoring (collecting data, preparation of reports)
- organize and maintain project files and keep database updated
Searching for and subsequently communicating with potential customers