Part-Time Clinical Research Coordinator – 9 Months (Turnhout)

IQVIA Inc; Brussel Hoofdstad; On-site; EUR 20,000 - 23,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator in Turnhout for an approximate 9-month engagement, requiring 8–10 hours per week. The role involves prescreening, data review, and supporting patient enrollment per protocol.

You will maintain study documentation and work with EDC/IRM systems, ensuring regulatory compliance. Ideal candidates hold a life sciences degree with clinical trial experience, strong IT skills, and excellent communication.

Qualifications

• Bachelor’s degree in life sciences or equivalent.
• Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules.
• Experience with lap samples and IRT/IWRS systems.
• Good knowledge of medical terminology.
• Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access).
• Must have 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.
• Fluency in English

Responsibilities

• Prescreening and Screening tasks
• Review charts from the site data base
• 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
• Lap 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

Skills

Clinical coordination

Data management

IRB familiarity

EDC systems

MS Office

Education

Bachelor's degree in life sciences

Tools

MS Office

IRT/IWRS systems

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator in Turnhout for an approximate 9-month engagement, requiring 8–10 hours per week. The role involves prescreening, data review, and supporting patient enrollment per protocol.

You will maintain study documentation and work with EDC/IRM systems, ensuring regulatory compliance. Ideal candidates hold a life sciences degree with clinical trial experience, strong IT skills, and excellent communication.