Clinical Research Coordinator

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Dijon, France.This role with an immediate start is for 24 hours per week and is expected to last around 7 months.The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documentsSupport with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.);Planning and coordinating logistical activity for study procedures according to the study protocolData entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completenessManagement and shipment of biological samplesPerforming ECG, taking vital signs, phlebotomyCoordinating with study monitor on study issues and effectively responding to monitor-initiated questionsAdministrative research taskWe are looking for candidates with:BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical professionGood knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedulesMust have at least 2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial siteBasic knowledge of medical terminologyStrong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and WordExcellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clientsGood organizational skills with the ability to pay close attention to detail If this sounds like the perfect opportunity for you, please apply now