drjobs Clinical Research Coordinator

Clinical Research Coordinator

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1 Vacancy
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Job Location drjobs

Herent - Belgium

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Are you looking for an opportunity to work with an industryleading company IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Diepenbeek near Hasselt.

This role with an immediate start is for 24 hours per week and is expected to last around 6 months.

The successful candidate 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.

As a pivotal member of the site team you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial including:

  • Maintaining uptodate 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 monitorinitiated questions
  • Administrative research task

We are looking for candidates with:

  • 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 indepth knowledge of departmental protocol and studyspecific 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 coworkers managers and clients
  • Good organizational skills with the ability to pay close attention to detail
  • Fluent Dutch language skills

If this sounds like the perfect opportunity for you please apply now!

#LICES

#LINS1

#LIHCPN

#LIDNP

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


Required Experience:

IC

Employment Type

Part-Time

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