Clinical Research Coordinator

4 weken geleden

Ede, Gelderland, Nederland IQVIA Voltijd
Job Title: Site Research Assistant

We are seeking a highly skilled and detail-oriented Site Research Assistant to join our team at IQVIA. As a pivotal member of our site team, you will play a crucial role in supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies.

Key Responsibilities:
  • Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Plan and coordinate 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
  • Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
  • Correct custody of study drug according to site standard operating procedures
  • Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions
Requirements:
  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
  • Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
  • 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
  • Fluent Dutch with good English language skills

If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity to join our team at IQVIA.

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