BrightOwl Loader Loading

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:
recruitment.germany@navitaslifesciences.com

Locations

Italy Italy

Find a Job Find Candidates

Similar Jobs

More jobs from Navitas Life Sciences

Other jobs in United States

Other jobs in Melbourne

Other Jobs

Most Recent Searches

Most Famous Searches

You might also like