Clinical Research Associate Ii H/F - PSI CRO

PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.You will:Conduct and report all types of onsite monitoring visitsBe involved in study startupPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team in preparing documents for study submissions

College/University degree in Life Sciences or an equivalent combination of education, training & experienceIndependent on-site monitoring experience in FranceExperience in all types of monitoring visits in Phase II and/or IIIExperience in oncology, hemophilia, infectious diseases, GIFull working proficiency in EnglishProficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travel