Senior Clinical Research Associate

A leading biopharmaceutical company in Paris is seeking a Clinical Research Associate II / Senior Clinical Research Associate to monitor clinical trials and ensure compliance with regulations. The role requires at least 2 years of independent monitoring experience, strong communication skills in English and French, and the ability to manage site...

Clinical Research Associate II / Senior Clinical Research Associate (France) Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA II) or Senior Clinical Research Associate (Sr. CRA) to join our A-team. As a CRA II / Sr. CRA at Allucent, you will independently control and monitor investigational...

We are expanding our team in France and are looking for an enthusiastic Senior Clinical Research Associate! GCP-Service International is a mid-size and privately owned independent full-service Contract Research Organization (CRO) founded in 2004 with headquarters in Bremen, Germany. Our satellite offices include locations in Siegburg (Germany), Prague (Czech

DescriptionRejoignez Excelya, où l’Audace, le Soin et l’Energie définissent notre identité et notre manière de travailler. Nous croyons en la création de solutions ambitieuses et en un environnement inclusif, où la collaboration et le développement individuel vont de pair.Dans le cadre du développement de plusieurs études interventionnelles,...

Êtes-vous le bon/la bonne candidat(e) pour cette opportunité ? Découvrez-le en lisant l'aperçu du poste ci-dessous.About the CompanyOur client, a leading player in the clinical research market, is currently seeking Snr CRA's to support long term sponsors across France.About the RoleAs a Senior Clinical Research Associate, you will have the opportunity to...

Company DescriptionCreated by Médecins Sans Frontières (MSF) in 1986, Epicentre carries out field epidemiology, training and medical research in support of MSF's humanitarian objectives. We have 3 research centres in France, Niger and Uganda and epidemiologists on site. Our areas of expertise cover infectious diseases (malaria, TB, HIV, cholera, Ebola,...

Direct message the job poster from Fortrea Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records Conducts site monitoring responsibilities for clinical...

Conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Essential Functions Complete appropriate therapeutic, protocol and clinical research training to perform job duties. Work with experienced

Experienced Clinical Research AssociateN'attendez pas pour postuler après avoir lu cette description ; un grand nombre de candidatures est attendu pour cette opportunité.OverviewAn opportunity is available for an experienced Clinical Research Associate (CRA) to support clinical trials within a sponsor-dedicated model. The role is responsible for monitoring...