Have you recently graduated and are eager to start your career in the fascinating world of Clinical Trials? Are you fluent in English and in Spanish? Are you hands-on, very communicative and highly motivated to start a new challenge? Don't look further, you've found your dream job!
Job description
One of our clients is looking for a Clinical Trial Associate to provide support to a big Postmarket Safety Surveillance Program in Medical Devices.
Responsibilities
- To provide support to a Postmarket Safety Surveillance program for 1 of their products
- A global program, this CTA is to provide support to sites in Europe
- Main tasks are to be in touch with the sites in order to collect data and images and to perform data entry.
- Lead of the project is based in the US.
- Some travel (once or twice a month) to sites
Profile
- Master in (Biomedical) sciences
- 1st experience with clinical studies via an internship is a plus (knowledge of specific regulations not needed)
- Very communicative, main tasks are to call sites, so not to be afraid to make phone calls
- To be able to work independent
- High level of English and Spanish
- Motivated and driven
- Existing right to work in Europe required
Benefits
- A balanced salary package based on your capabilities and experience
Vacancy number : 18052
