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...
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulatio...
My client is a global leading CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. ...
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...
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. ...
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. Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. Selecting inves...
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. ...
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. ...
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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