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...
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...
AL Solutions is working with a global contract research organization (CRO) specializing in providing clinical research services to pharmaceutical, biotechnology, and medical device companies. We are currently seeking a highly motivated Clinical Research Associate. Minimum of 2 years of experience as...
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...
My client is a global leading CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. ...
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...
Assurer dans le cadre de multiprojets, la liaison avec d'autres chefs de projet et la gestion des interfaces. De formation supérieure, vous avez au minimum 3 ans d’expérience en gestion de projets, sur des chantiers TCE, idéalement en positionnement de maitrise d’ouvrage (vous aurez en gestion des m...
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