Clinical Research Coordinator - Turnhout

QPL IQVIA RDS Poland Sp. z o.o.; 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

Clinical Research Coordinator in Turnhout

Working Hours: 8-10 hours per week Start Date: Immediately Duration: Approximately 9 months

Key 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

Your Profile

• 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 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
• Strong organizational skills and attention to detail
• Fluency in English #LI-HCPN #LI-CES #LI-DNP #LI-NS #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.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.

Learn more at https://jobs.iqvia.com