Chloe O'Shea has a brand new and fantastic opportunity for Senior CRA's in the France! Chloe is working with a global CRO who are looking for dedicated Senior CRA's to join their close-knit team! The successful candidate will have lots of autonomy and will have a lot of say in the clinical trials so...
As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. ...
We are looking for a Clinical Research Associate II (CRAII) to join our A-team (hybrid*/remote). As a CRAII at Allucent, you will independently control and monitor investigation sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial proto...
Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines. Parexel is currently seeking a Clinical Research Associate II in France. Working as a Clinical Research Associate II at Parexel FSP offers tremendou...
My client is a global leading CRO who has demonstrated a commitment to innovation, quality, and collaboration in the clinical research industry. ...
Clinical Research / Clinical Trials / Remote Work / GCP / Regulatory Compliance / Pharmaceutical / Life Sciences / Clinical Monitoring / Contract Research Organization / Clinical Data / Patient Safety. As a Contract Clinical Research Associate, you will play a pivotal role in advancing clinical tria...
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...
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...
You would like to be engaged in the company training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice and applicable regulatory requirements. Complete appropriate...
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