What your responsibilities will be- You will provide operational support for global pharmacovigilance activities of Grifols marketed products- You will ensure pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines- You will be responsible for data review, compilation and analysis including management of the integrated safety database- You will manage Adverse Events including activities such as processing adverse event case reports and conducts follow-up- You will notify regulatory agencies and business partners accordingly;
responds to requests from regulatory agencies- You will draft and review periodic safety update reports#J-18808-Ljbffr