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...
We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural documents, inte...
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. ...
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...
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. ...
As a Clinical Research Associate. ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Planni...
My client is a global leading CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. ...
Clinical Research Associate Lead – M/F. You hold a Master’s degree in Clinical operations or related field. You have at least 5 years of professional experience in Clinical operations. ...
Responsibilities will be dependent upon the type and timing of the program to which the Senior CRA is assigned and will, at a minimum, include start-up and study implementation activities, on-site monitoring of clinical research studies as well as on-going site management. Incumbents are expected to...
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