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.