Pharmacovigilance Associate


KLIFO is looking for a talented and committed Pharmacovigilance Associate based in Denmark

KLIFO is expanding our office in Denmark and wants to engage an additional Pharmacovigilance Associate into a dynamic and experienced team within Pharmacovigilance Solutions. The person we want to engage like to work in an a consulting environment and has a positive, proactive, flexible, self-driven and self-confident personality. We can offer a highly flexible, free and trustful working climate with exciting customers and projects among competent colleagues where your knowledge, experience and contribution are valuable and highly appreciated.

The position:

The Pharmacovigilance Associate is responsible for collaboration with clients and execution of projects according to the clients expectations:

  • Single Adverse Event case handling including data entry, evaluation, assessment and writing of safety narratives
  • Monitoring of the pharmacovigilance mailbox
  • Handling of safety databases
  • Preparation of pharmacovigilance and safety documents; for example Safety Management Plans, PSURs, DSURs, and safety signal reports
  • Drive medical monitoring activities
  • Maintain pharmacovigilance system master files
  • Author and review of SOPs

Qualifications:

  • MSc/BSc in the life science field, nurse or holding a diploma within Pharmacovigilance
  • Preferably > 3 years of experience from a similar position in the pharmaceutical industry/Biotech/CRO
  • Knowledge og drug safety guidelines, terminology and processes
  • Experience with safety databases
  • Excellent communication skills in English both written and verbal
  • Experienced user of MS Office and good understanding of databases
  • Able to translate client´s needs into solid deliveries

We offer:

  • Work within different therapeutic areas and with tasks of varying complexity
  • Work with a heterogeneous client pool (pharmaceutical companies, stablished biotech, newly started biotech and academia)
  • Build international client relations
  • Use and elaborate your competences and experience
  • Work in an interactive, flexible and positive working environment

Location:

KLIFO has offices in Denmark, Germany, Sweden and the Netherlands. This position is located at our office in Glostrup, Denmark

Contact:

For more information, please contact Randi Rahbæk, Senior Clinical Director  at +45 4477 8704

Applications should be sent to: moc.ofilk@boj marked Pharmacovigilance Associate

KLIFO processes your application and all related personal data exclusively for the specific hiring process. Your data is processed as confidential information, cf. the current data protection law (GDPR).

Deadline: Please reply as soon as possible. Recruitment interviews will be held on an ongoing basis.

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