Clinical Research Associate

vor 2 Wochen

Graz, Österreich QPS, LLC Vollzeit

**What will you do?** In this role, you will monitor clinical drug studies across various research centers according to applicable guidelines such as GCP and WMO. You will manage studies from site initiation to close-out, communicate with clients, conduct regular site visits, and write reports. You will verify data, check study drug accountability, discuss study progress and issues with site staff, and review various aspects of execution, processes, samples, and materials. You will verify that any and all adverse events are processed properly. You will write site visit reports and track your sites' progress regularly to the study team and sponsor. Monitoring activities will primarily take place at clinics in Groningen and Leeuwarden. You will work as part of our Clinical Operations team yet also independently during visits to research centers. The hours are flexible, and you will work from home when not traveling to the site. **Work Location** Netherlands, Groningen; ask about our flexible work options. **Who are you?** Ideally, you have a bachelor's degree, or an academic level obtained through education and/or experience with a (para)medical or biological background. Prior clinical trials monitoring ("CRA") experience is ideal (as this is a challenging job and requires depth of knowledge in the field). You are expected to work precisely and organized, and to communicate effectively. You are proactive with an eye for detail. You have a good command of English, spoken and written, as that language is needed for internal communications plus with clients/sites/sponsors. **Vaccination protocol** **What do we offer?** We offer a varied role within a dynamic and international organization. We provide a full-time position of 32-40 hours per week for at least one year. After one year, there may be an opportunity for extension. **Want to know more?

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