Clinical Research Associate

Clinical Research Associate

Key responsibilities:

  • Site management including regular contact with involved site, collecting of essential documents, writing reports, handling of questions, follow-up actions and reporting to 1MED project manager;
  • Whenever applicable perform site evaluation visits;
  • Site initiation, monitoring and close out services, including support of the site in their responsibilities and preparing on-site archiving;
  • Assist project manager on assigned projects and will take a lead role where required.

 

Qualifications:

  • CRA certification according to the MD 15/11/2011;
  • Previous experience as CRA with monitoring experience of (at least) 1 year;
  • Fluency in English and Italian is a must;
  • Location: home based in Milan/Como area;
  • Experience in Medical Device trials is preferred;
  • Must be able to travel in accordance with company and project requirements;
  • Good interpersonal skills demonstrated as proactive, enthusiastic, flexible, collaborative, problem solver and independent thinker.

 

 

Please fill in the form below and send us your CV.

    Please review our Privacy Policy for more details

REGULATION (EU) 2017/745

REGULATION (EU) 2017/745