Clinical Research Coordinator

**Job Summary**

IQVIA is seeking a highly skilled and detail-oriented Clinical Research Coordinator to support a clinical research study at a site in Venlo. As a pivotal member of the site team, you will be responsible for maintaining a safe study environment and ensuring the smooth running of the clinical trial.

Key Responsibilities:

• Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
• Perform ECG and take vital signs.
• 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.