Site Research Assistant - Dijon, France
- Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
- Support 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 protocol
- Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
- Management and shipment of biological samples
- Performing ECG, taking vital signs, phlebotomy
- Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
- Administrative research task
- 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 profession
- Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
- Must have at least 2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site
- Basic knowledge of medical terminology
- Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
- Good organizational skills with the ability to pay close attention to detail
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