Description
IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Turnhout. This 8-10 hour per week role 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:
- Prescreening and Screening tasks
- Review charts from the site database
- Maintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and eTMFs
- Supporting patient screening and enrollment, including handling informed consent and privacy documentation
- Lab sample processing and shipment
- Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations
- Patient scheduling support
- Coordinating logistical activities for study procedures in line with the study protocol
- Communicating with study monitors and responding to study-related inquiries
- 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:
- 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)
- Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
- Experience with lab samples and IRT/IWRS systems
- Good knowledge of medical terminology
- Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
- At least 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 English