About the Role
Do you like to coordinate and monitor (inter)national, multicentre clinical trials in order to assure the quality of the clinical data? Then this could be the opportunity to develop your career at our Scientific CRO.
We are actively looking for a talented and proactive Clinical Research Associate with strong communication and coordination skills and with willingness to travel on an irregular base.
You will be part of the CRA team, currently existing of 20 CRA’s, and you will report to the Manager Clinical Operations.
Tasks and responsibilities of the Clinical Research Associate
- Monitor clinical research in accordance with the protocol, SOPs, applicable laws and ICH-GCP guidelines, including visit report compilation and follow-up within the set timelines;
- Perform feasibility, site selection, initiation, monitoring and close out visits in accordance with contracted scope of work, using good clinical practice...
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Submit your application today and take the next step in your career journey with Julius Clinical.
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