The Clinical Research Associate II monitors investigational sites to ensure subject safety and provides high quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/ International Conference on Harmonization (IC...
Taylor Young has partnered with a global CRO looking for an experienced Clinical Research Associate or senior to expand their Clinical Operations team in France. ...
The Clinical Research Associate (CRA) conducts clinical monitoring tasks at trial sites, ensuring adherence to ICH guidelines, GCP, local regulations, and SOPs. Clinical Research Associate - France. On behalf of our client, a pharma-biotech company developing innovative oncology medicines, we are se...
We are currently seeking multiple experienced Senior Clinical Research Associates to join our client’s expanding Clinical Operations team in Romania. Minimum of 4 years of experience as a clinical research associate in the pharmaceutical or CRO industry. Client Overview: Our client is a leading glob...
Working alongside the Project Management Team, oversees performance of assigned Clinical Research Associates (CRAs)/ Clinical Site Specialists (CSSs) and site activities in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines, Clinical Trial directives, Europea...
My client is a global leading CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. ...
You have a scientific degree (minimum Bac +5), completed by a specific Clinical Research Associate training. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Excelya is a...
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