The tasks as Pharmacovigilance Associate in Teva Global Pharmacovigilance Data Management Unit Romania mainly consist of :
Adverse event reports processing including MedDRA coding, seriousness assessment, duplicate searches, distribution and submission of expedited reports to the relevant authorities
Taking part of departmental projects as a core team member, providing data management input for different areas of expertise like data entry conventions
Being part of different working groups
Interacting with all PhV functions
Taking part in the development and maintenance of an efficient and robust Pharmacovigilance system
The ideal candidate should have :
University graduate (Pharmacy, Veterinary Medicine, Biology)
Fluency in both written and spoken English
A good understanding of medical concepts and a confident user of English medical terminology
Easiness to communicate in English with foreign colleagues and business partners
Adaptability to routine activities but also to finding fast answers and solutions to unexpected situations
Willingness to quickly learn and develop in a multicultural team of highly skilled professionals
Good computer skills (Office-Excel, Word, PowerPoint; Outlook)
Pro-active, punctual, well organized and responsible person
Flexible and open attitude
A team player but also enjoy working independently
We offer :
An exciting and challenging job in an innovative, flexible, and growing company
A team of young, hard-working, open-minded and friendly colleagues
Initiation and trainings in Pharmacovigilance field reflecting the latest European requirements
Function Regulatory Affairs Sub Function Pharmacovigilance Already Working TEVA?
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