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(PV) Associate (m/f)
O poslu
As a result of our rapid growth we are looking for:
Pharmacovigilance (PV) Associate
The PV Associate should be a Life Science graduate (Faculty of Medicine, Faculty of Pharmacy and Biochemistry, Veterinary Faculty) or have equivalent nursing or medical qualifications.
The Pharmacovigilance (PV) Associate tasks will include:
• To perform initial triage of the received safety notifications
• To process Individual Case Safety Reports (ICSRs), including data entry in ArisG safety database
• To follow-up ICSRs with the reporter, generate follow up (FU) queries and send FU requests
• To carry out ICSR local regulatory reporting, perform expedited reporting (including electronic reporting) and periodic reporting
• To perform ICSR reconciliations with business partners
• To review literature screening search results, identifying ICSRs and other safety-related findings.
• To write or contribute to PSURs and DSURs as required. This may include acting as the project co-ordinator, collating the needed information, incorporating reviewers’ comments and finalizing the document.
• To assist with pharmacovigilance processes, supporting preparation of SOPs, product safety reviews, as required.
O zaposleniku
- excellent English skills (both verbal and written)
- excellent French, German, Spanish or Italian skills (both verbal and written)
- excellent IT skills (MS word, Excel)
- ability to manage multiple and varied tasks and prioritize workload with attention to detail
- excellent interpersonal and communication skills
- willingness to work in a international matrix environment and to value the importance of teamwork
We offer:
- full-time position
- salary negotiable
- stimulating working environment
- opportunity for career development in a fast growing healthcare company
Please send us your motivation letter and your CV in English to [email protected]
Only short-listed candidates will be contacted.

