Senior Clinical Research Associate. At Metric Search we're partnered with a leading global CRO that are currently expanding their Clinical Operations team extensively across Europe, with a focus on building out the CRA team within France. Coordinate the logistics in relation to shipment & storage of...
August Research, An Everest Clinical Research Company, is looking for an experienced Clinical Research Associate (CRA) in France. Job responsibilities will include site identification and site selection, assisting in performing regulatory and ethics committee submissions, monitoring for clinical stu...
Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in clinical system...
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...
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...
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. ...
My client is a global leading CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. ...
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...
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