Company: Anglo-Spanish Contract Service Company specializing in Epidemiology, Pharmacovigilance, Health Economics and Quality of life is seeking a candidate to expand its pharmacovigilance activities.
Requirements:
S/he will be responsible for follow-up, querying, collecting and entering ICSRs (cases) in databases; expedited reporting to Eudravigilance, other European Regulatory Authorities and Ethical Committees; and distribution of SUSARs to investigators. S/he will also help in safety related matters such literature searches, safety reports, safety reviews, training, SOPs and WIs.
Training will be provided as necessary, including analyses of FDA(AERS)and WHO (Vigibase) adverse events databases
Contract: Full time
Start date: October 2010 (immediate)