Clinical Research Associate

2 weken geleden


Amsterdam, Noord-Holland, 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 one or several sites in Amsterdam.

About the Role

This freelance role is for 16-40 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
  • 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, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession
  • Qualified and competent in ECG and vital signs
  • 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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