Associate III, Drug Safety (m/f/t/i)

  • 85737 Ismaning, Germany
  • Full-time
  • Department: Research & Development
  • Region: EU+/Canada

Job Description

We are looking for an Associate III. Drug Safety,

office-based, contract via temp vendor
in Munich
full-time, maternity cover, first for 12 months
team: diverse (about 10)
Start: as soon as it possible

Key responsibilities:

Support Drug Safety team in administration of adverse event and pregnancy reports (incl. follow up)

Recognition, documentation and reporting of adverse events and technical product complaints to Drug Safety Germany or the responsible service provider according to local SOPs.

Drug Safety

·        Collection, documentation and any further processing of adverse event and pregnancy reports

·        Affiliate triage of incoming safety reports

·        Data entry in electronic systems

·        Following up on safety reports

·        Cooperation with Global PV Department and case processing vendors

·        Training of new safety associates, as needed

Qualifications

Education:

• Degree in pharmacy or life sciences,
• or Medical documentation specialist,
• or Registered nurse,
• or Medical-laboratory assistant,
• or Pharmaceutical assistant
• and chemical-technical assistant

Skills:

• At least 1 year working experience in pharmacovigilance/drug safety (special focus: data entry, triage and tracking of safety reports)
• Preferably medical background: degree in nursing, pharmacy, or other health care related profession (like PTA) or life sciences required
• Fluency of German and English
• Knowledge of medical terminology in German and English
• Attention to detail and accuracy
• Ability to multi-task and prioritize
• Must work effectively/collaboratively in a fast-paced team environment
• Ability to work independently

 

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