Clinical Research Associate

4 weken geleden

Breda, Noord-Brabant, Nederland IQVIA Voltijd
Join Our Team as a Clinical Research Coordinator

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are currently seeking a highly skilled Clinical Research Coordinator to support a site in Breda.

About the Role

This freelance role is for 16 hours per week and is expected to last approximately 12-17 months. As a Clinical Research Coordinator, you will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.

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.
  • ECG and vital signs.
  • 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, 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.
  • 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.

#LI-CES

#LI-NS1

#LI-DNP

#LI-HCPN

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