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...
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...
My client is a global leading CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. ...
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...
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. ...
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...
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. ...
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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