• Company:
  • Job Location:
  • Date: January 27, 2021 03:12
  • Employment Type: Any
  • Experience: Any
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Job summary

We're looking for a candidate to fill this position in an exciting company.Planning, executing and reporting of studies according to applicable regulatory requirements and company procedures;...

Job description

We're looking for a candidate to fill this position in an exciting company.

  • Planning, executing and reporting of studies according to applicable regulatory requirements and company procedures; including study protocol preparations, start-up activities at study sites, ethical approvals, study monitoring, and reporting of results
  • Acts as a member of a project team to contribute towards efficient management of clinical studies
  • Monitoring of global clinical evidence requirements and development of internal clinical study management procedures
  • Additional responsibilities may include tasks within Regulatory Affairs

  • MSc degree or equivalent in bioscience
  • Experience in clinical studies, preferably related to In Vitro Diagnostic
  • Knowledge of IVDR (Regulation 2017/746) preferred; basic knowledge required
  • Excellent organization and communication skills
  • Independent, self-directed person to be able to multi-task in fast pace environment and in global team environment
  • The work will involve some travelling, mostly in Europe
  • Excellent skills in Finnish and English

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