Clinical Research Coordinator Beek

Clinical Research Coordinator Beek (Part-Time24 hours/week some remote work possible)

Start Date: Immediate
Duration: Approximately 6 month

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Beek. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

Key Responsibilities
As a vital member of the site team you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks including:

• Maintaining up-to-date study protocols case report forms (CRFs) Electronic Data Capture (EDC) systems and other study documents
• Support with screening and enrolment of patients and collection of related documents (informed consent privacy consent etc.);
• Planning and coordinating 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
• Management and shipment of biological samples
• Performing ECG taking vital signs phlebotomy
• Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
• Administrative research task

Your Profile
We are looking for candidates who bring a combination of education experience and skills:

• Bachelors degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g. clinical research coordinator research assistant nurse medical assistant)
• Solid understanding of clinical trials and familiarity with study protocols consent forms and schedules
• good knowledge of medical terminology
• Strong IT skills including proficiency in MS Office applications (Outlook Word Excel Access)
• Must have at least 1-2 years experience working as a Clinical Research Assistant Research Nurse or Clinical Research Coordinator at a clinical trial site
• Excellent interpersonal and communication skills
• Strong organizational skills and attention to detail
• Fluency in Dutch and good command of English

Why Join IQVIA
At IQVIA you will be part of a global team that is advancing healthcare through data technology and human science. We offer a supportive work environment impactful projects and the opportunity to make a real difference.

Interested
If this sounds like the right opportunity for you we encourage you to apply today.

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IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at