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