Responsibilities

  • Data entry of vigilance cases in the relevant databases
  • Preparation of initial email (in the context of follow up request), requests for clarification
  • Submission of cases to the competent authorities
  • Carrying out specific queries in the databases in order to draft reports
  • Monitoring and downloading ICSRs in the national databases (Eudravigilance, MHRA portal)
  • Monitoring a generic mailbox and support in the registration and the initial triage in the database
  • Quality control of vigilance cases
  • Recordings/updates on XEVMPD
  • Drafting/updating of technical agreements /safety management plan /client template
  • Drafting/updating of SOPs/WPDs/Trainings others documents directly related to their activity
  • Participation in the implementation/maintenance/improvement of processes

Education & Experience

  • Bachelor’s degree in science related field
  • Fresher or 1 year of PV experience
  • Well versed with Outlook and Microsoft Office

Skills

  • Database experience preferred
  • Process oriented
  • Enjoys working with documentation
  • Good computer skills
  • Works well within a team
  • Knowledge of medical terminology
  • Organized
  • Flexible
  • Excellent communication skills in English and French

Publish Date

07 November, 2024

Spontaneous Application

Data Officer (Pharmacovigilance) 503

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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