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Clinical research coordinator / study nurse - alken, belgium

Hasselt
Publiée le 8 octobre
Description de l'offre

Clinical Research Coordinator / Study Nurse – Alken, Belgium (Part-Time, 24 hours/week)


Start Date: Immediate
Duration: Approximately 6 months

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Alken, Belgium. 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:

1. Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
2. Supporting patient screening and enrollment, including handling informed consent and privacy documentation
3. Coordinating logistical activities for study procedures in line with the study protocol
4. Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
5. Managing and shipping biological samples
6. Communicating with study monitors and responding to study-related inquiries
7. Carrying out general administrative tasks related to the study

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

8. Bachelor’s 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)
9. Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
10. good knowledge of medical terminology
11. Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
12. Must have at least 1-2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site
13. Experience in collecting patient vital signs and laboratory samples, administering investigational products, and conducting electrocardiograms (EKGs) is considered an advantage
14. Excellent interpersonal and communication skills
15. Strong organizational skills and attention to detail
16. 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.

#LI-HCPN

#LI-CES

#LI-DNP

#LI-NS1

#LI-Onsite

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

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