Study Startup Coordinator

1 mese fa

Milan, Italia PSI CRO A tempo pieno
Job Description

Take your career to the next level and be involved in clinical study startup processes in Italy. You will provide operational support to project teams and ensure that PSI clinical projects start smoothly and on time. 

You will:

  • Perform administrative activities related to the clinical study startup process in Italy: documents collection/distribution to hospitals, translation of startup documents, filing, database (CTMS) maintenance, minutes keeping
  • Provide regular site startup progress updates to project teams
  • Coordinate preparation of initial submission dossiers to competent authorities, ethics committees, and/or site submission dossiers
  • Prepare IP-RED packages
  • Monitor startup key performance indicators for the assigned projects

Qualifications

  • College/University degree 
  • Prior experience in an administrative role in international environment
  • Prior experience in clinical research industry 
  • Full working proficiency in English and Italian
  • Communication and organizational skills
  • Attention to detail
  • Ability to work in a team or independently


Additional Information

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. Advance your career in clinical research and develop new skillsets whilst growing with the organization

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