ágnes diviánszky
pharmacovigilance quality
About
Mainly responsible for single case data entry quality control to improve the data quality of Individual Case Safety Reports by performing appropriate corrections, documenting the results of quality check and giving summarized and individual user feedback.
hungary
hungary
pharmaceuticals
food, nutrition, public health, life sciences, healthcare, research, medicine, powerpoint, english, microsoft excel, teamwork, microsoft office, public speaking
Experience
pharmacovigilance quality
pharmacovigilance quality reviewer
tata consultancy services
research assistant
hungarian dietetic association
research assistant
university of physical education research institute of sport sciences
research student
semmelweis university department of neurology
research student
university of debrecen institute of physiology
volunteer
organisation of conscious consumers
pharmacovigilance case processor
tata consultancy services
* Main responsibilities include: * Entering serious and non-serious adverse events regarding initial and follow-up safety reports onto PV safety database according to Client’s rules and manuals by priority and considering the due dates for completion to avoid compliance issues * Extracting relevant information from routine source documents and/or information coming from the Client affiliates via LAM or from E2B messages * Assessment of seriousness, global listedness and causality of serious and non-serious adverse events * Creating comprehensive case descriptions in English extracting relevant information from source documents * Checking of incoming PV information for consistency and completeness and requesting clarification/additional information from Bayer affiliates and/or subcontractors within set timelines, as detailed in Client’s global SOPs * Verifying the accuracy of MedDRA and WHO-DD coding of reported adverse events and concomitant drugs
Education
semmelweis university
semmelweis university
ágnes diviánszky's Contact Information
Phone
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