Skip to main content

Pas encore prêt à postuler ? Rejoignez notre Global Talent Network.

Job Description

Clinical Research Coordinator - Groningen

Groningue, Pays-Bas R1455699

Groningue, Pays-Bas

POSTULER

Description du poste

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Groningen.

This role is for 21 hours per week and is expected to last approximately until beginning of April 2025.

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 up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Perform ECG and take vital signs
  • 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
  • Assisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
  • Correcting custody of study drug according to site standard operating procedures
  • Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions

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

    #LI-CES

    #LI-NS1

    #LI-DNP

    #LI-HCPN

    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 https://jobs.iqvia.com

    POSTULER

    En Savoir Plus Sur Notre Facon De Travailler

    Learn About How We Work

    POSTES SIMILAIRES

    Afficher toutes nos offres VOIR PLUS DE POSTES

    Rejoignez notre Global Talent Network.

    Restons connectés. Inscrivez-vous pour être informé(e) des nouvelles opportunités correspondant à vos souhaits de carrière.

    Rejoignez notre réseau