Clinical Research Coordinator

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Tiel.

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 documents
• Perform ECG and take vital signs
• Planning and coordinating logístical 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
• Assisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
• Correcting custody of study drug according to site standard operating procedures
• Coordinating with study monitor on study issues and effectively responding to monitorinitiated questions
• 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 indepth knowledge of departmental, protocol and studyspecific operating procedures, consent forms, and study schedules
• Basic knowledge of medical terminology
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with coworkers, managers and clients
• Good organizational skills with the ability to pay close attention to detail
• Fluent Dutch with good English language skills

Job Type:
Contract

Work Location:
In person

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