Clinical Research Associate

1 maand geleden

Groningen, Nederland QPS Voltijd

**What will you do?**

In this role, you will travel to and 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 work as part of a team but also independently during visits to research centers. When not traveling to a clinical trial site, you will work from home.

**Who are you?**

To qualify for this role, you’ll need extensive, hands-on experience managing all facets of clinical trial monitoring as a Clinical Research Associate. Ideally, you hold a bachelor’s degree or an equivalent academic level, obtained through education and/or experience, with a (para)medical or biological background. We seek a detail-oriented professional who works with precision and organization and communicates effectively. Proactivity and an eye for detail are essential. Proficiency in both Dutch and English, spoken and written, is required. You must also be able to travel to assigned clinical trial sites, which may occasionally involve overnight stays.

**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. You will also have the opportunity to work from your home office in the Netherlands or Austria

**Want to know more?**

**Vaccination protocol

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