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International Open Positions

With 530 years of heritage, more than 3.000 employees, a leading Research and Development Center and two major production sites in Prague and Bucharest, Zentiva strives to be the champion of Generics to support the daily healthcare needs of people living in Europe.The growth of our organization brings new opportunities for our people to fulfil their potential. It also positions us well to attract the best talent and retain our team to secure our success for future generations. Join us!

Drug Safety Expert

Your responsibilities:

  • Drug safety evaluation during post-authorization period; Analysis of internal (case reports) and external (scientific literature) data
  • Elaboration of safety related parts (benefit-risk, epidemiology) for pharmacovigilance documents (Periodic Benefit Risk Evaluation Report, Addendum to the Clinical Overview, Risk Management Plan)
  • Participation in signal management process; Evaluation of the association between drug exposure and adverse event occurrence
  • Participation in case management process
  • Medical review of ICSRs
  • Participation in routine Pharmacovigilance activities
  • Effective communication with relevant stakeholders

We require:

  • University degree MD (preferably) or PharmD.
  • Previous experience in pharmacovigilance or clinical practice is advantageous
  • Proven excellent communication and organization skills
  • Interest in the area of pharmacovigilance
  • Willingness and desire to learn new things
  • Advanced level of English
  • Strong PC skills
  • Detail oriented, hardworking personality
  • Team player

We offer:

  • Challenging career opportunity to work for a successful international company
  • Opportunity to broaden your knowledge and expertise in your field
  • Possibilities for own personal growth and further language development
  • Competitive remuneration and wide portfolio of employee benefits
  • Above-standard social, healthcare and educational program

Contact

Zentiva
Klára Pavlíková