Pharmacovigilance Associate Amsterdam

Deze vacature staat offline!

De opdrachtgever

Farmaceutisch bedrijf in Amsterdam.

De omschrijving

  • Develop and implement local procedures relative to pharmacovigilance, and training of local affiliate staff
  • Guarantee PV business continuity by ensuring management of PV processes and PV coverage and feedback back-up coverage
  • Collect safety data and other PV-related responsibilities and screen local literature
  • Track, report and follow up of adverse events, ICRs through organized data collection programs
  • Provide safety information required for preparation of periodic safety report, upon request to SST
  • Act as backup ASR and fulfill National Regulatory Authority regulations with respect to pharmacovigilance (PV)
  • CGR document review and approval for the local affiliate

De eisen

  • MSc, medical biology or similar relevant scientific education, prior role as Clinical Research Associate and/or in clinical development is an advantage.
  • Bilingual NL/EN
  • Min 5 years experience in a similar role/environment
  • Good planning and organisational skills
  • Sense of duty, responsibility and accuracy
  • Able to translate PV policies and procedures into a understandable and practical language in order to ensure adherence to the PV policies of this company
  • Autonomous but able to work with peers and business contacts

De arbeidsvoorwaarden

Uitstekende arbeidsvoorwaarden.


Heb je interesse in deze vacature, meld je direct aan middels de button 'aanmelden' of neem contact op met:
Dr. Arjan van den Wijngaard
Consultant Medical
Goeman Borgesiuslaan 77
3515 ET Utrecht
tel 030 231 7350
mobiel 06 50650550