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Clinical Research Coordinator

2 maanden geleden

Ede, Gelderland, Nederland IQVIA Voltijd

Job Summary:

IQVIA is seeking a highly skilled and detail-oriented Clinical Research Coordinator to support a clinical research study at a site in Ede. As a pivotal member of the site team, you will be responsible for maintaining a safe study environment, ensuring compliance with health and safety policies, and supporting the clinical trial team.

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.
  • Enter data, perform data quality checks, and resolve queries 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.
  • Correctly manage 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.