Clinical Research Associate, France

Job OverviewConduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.External Job DescriptionJob OverviewConduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable...

Fortrea in Paris is seeking a Senior Clinical Research Associate II (SCRA II) to oversee site visits, ensure GCP compliance, and drive trial integrity within the FSP department. You will manage sites, perform SDV, and train investigators, contributing to robust trial execution and data quality.Join a dynamic team in Paris offering a collaborative...

Senior CRA At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients...

Senior CRAAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients...

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.As a Clinical Research Associate (CRA), you will be responsible for monitoring clinical studies and ensuring compliance with study...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at...

IQVIA is seeking a Clinical Monitoring professional to conduct site visits in accordance with the study protocol, GCP and regulatory requirements. You will coordinate with experienced staff and manage monitoring activities across assigned sites.Responsibilities include training site staff, maintaining TMF and ISF, tracking regulatory submissions, recruitment...

Company Description Medicine moves forward here. So will you. Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize...

Fortrea’s Paris office is seeking a Senior Clinical Research Associate II (SCRA II) to monitor clinical trials, oversee site operations and ensure GCP compliance across France. The role involves site visits, data verification, and collaborating with investigative sites to maintain study integrity.Responsibilities include SDV, investigator training, and...