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We are looking for colleagues with a life-science background, nursing or other healthcare-related areas. If you do not already have experience in the field of (pharmaco-) vigilance we offer thorough training on the job by experienced colleagues.

Safety Specialist

Overview of Job Function:

  • If a side effect is reported, it is the Safety Specialist’s responsibility to compile the available information, to enter the information into the safety database and eventually to conduct the timely submission to competent authorities (e.g. FDA)
  • Furthermore, the Safety Specialist assumes the role of a Safety Writer when compiling aggregate analyses of the available safety data.

Specific tasks of the Safety Specialist /
Safety Writer include:

  • Data entry into the safety database
  • Submission of reportable case reports to competent authorities (e.g. FDA)
  • Generation of line listing
  • Conduction of literature searches
  • Generation of aggregate safety reports (e.g. PADERs, PBRERs)
  • Generation of Standard Operating Procedures (SOPs)

Desired Qualifications and Skills:

  • Bachelor or Master Degree in Life-Sciences, Nursing or other Healthcare-related Degree, or similar qualification
  • Good understanding of scientific data and the ability to compile a meaningful and concise narrative and report
  • Attention to detail and a high level of accuracy
  • Candidate should have excellent communication skills, a strong focus on teamwork and should enjoy working in an international environment

Please send application / resume to: