Pharmacovigilance Associate in Zagreb (Croatia)

Where: Zagreb (Croatia)

Extent of Work: Full Time

Click here to apply in English

Based in our office in Zagreb (Croatia), the (PV) Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance clients.

Key Accountabilities:

  • Perform initial triage of the received safety notifications
  • Process Individual Case Safety Reports (ICSRs), including data entry into the IRT ArisG safety database
  • Follow-up ICSRs with the reporter, generate follow up (FU) queries and send FU requests
  • Handle technical product complaints
  • Perform ICSR reconciliations with business partners
  • Review local literature screening search results, identifying ICSRs and other safety-related findings

Qualifications and Skills:

  • Educated to degree level or above in life sciences or a related field
  • Good understanding of Pharmacovigilance
  • Fluent knowledge of English (written and oral) plus Slovenian, Dutch or Swedish language is a must
  • Advanced knowledge of MS Office (Word, PowerPoint, Excel)
  • Excellent interpersonal, verbal and written communication skills
  • Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives
  • Ability to work effectively in an international matrix team and value the importance of teamwork

Our offer:

  • Work within a successful, highly – qualified and dynamic team
  • Professional training and career development in a fast growing healthcare company. – Pharmacovigilance (PV) Associate – Slovenian, Dutch or Swedish speaking (m/f) – Zagreb – PrimeVigilance Zagreb d.o.o.


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