Responsibilities

  • Ability to take QPPV
  • To support the QPPV
  • Ability to support in PV audit/inspection
  • Ability to take on GPO (graduated plan officer) or local PV person responsibilities : − Main contact and communication for health authority and the MAH. − Nomination of the details with the local health authority − Revison of PhV contracts − Monthly reconciliations with partners − Weekly or monthly (depending on the frequency of publication)surveillance of local journals − Monthly surveillance of local Health Authority website for identification of safety related data.

Required Education

Life sciences degree (vigilance, Pharmacist or medical degree is a plus)

Required Experience

2-15 years of experience in Pharmacovigilance/drug safety

Required Languages

German speaker any other European language would be desirable.

Required Technical Skills

  • Ability to take on GPO responsibilities (Stufenplanbeauftragter)
  • EU GVP and ICH/GCP understanding
  • Agility and analytical
  • Proficiency in professional and technical Organization, initiative, anticipation and adaptability
  • Good interpersonal skills, team player and excellent communication skills
  • Ability to attend customer facing teams & F2F meetings

Additional Experience/Skills

  • 2-6 years of experience as a drug safety or Pharmacovigilance department/industry
  • Experience in case management or medical information and literature or medical writing in German or English
  • Knowledge of the relevant German regulation and EU GVP
  • Experience as a deputy GPO or (Stufenplanbeauftragter) or working closely with the QPPV office would be an advantage

Publish Date

24 August, 2023

Spontaneous Application

Vigilance Specialist 963

New opportunities open up across PLG all the time. If nothing matches right now, send us a spontaneous application: we will keep you in mind for what comes next.

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