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Senior Clinical Research Associate (IT sites) Melbourne United States,  

Navitas Life Sciences (company)

Posted on : 22 December 2017

Project Description

Location: Italy

Job Description:

  • Monitor clinical trials in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines. This will comprise performing pre-study-, initiation-, monitoring- and close out-visits.
  • Communication with investigational sites to improve trail conduct and to strengthen motivation of site staff involved in projects
  • Creating study relevant documents for submissions to competent authorities and ethics committees
  • Be up to date with European and local regulatory requirements in clinical trials
  • Participation in national and international project and investigational meetings

Preferred Skills:

  • At least 5 years of experience as a CRA
  • Team player with strong communication and collaboration skills
  • Ability to work with investigational sites in Denmark, Norway and Sweden
  • Excellent at planning, organising and executing trial activities
  • Ability to prioritize tasks, while keeping attention to important details
  • Study of natural science (biology, medicine, pharmacy or nursing) or equivalent
  • Willingness to travel

If you would like to apply for this position, or would like a discussion about this, or any other role, please send your contact details, together with your curriculum vitae to:


Italy Italy

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