Senior Clinical Trial Assistant, Sponsor Dedicated - Belgium
- LocationBrussels, Brussels-Capital Region, Belgium
- Work typeNot stated
- EmploymentFull-time
- Posted6 November 2026
- SourceIqvia's careers page (Workday)
Live checkFirst seen 7 h ago; still listed on Iqvia's careers page 3 h ago.
Moves fastWhen Iqvia takes a role down early, it is usually about 2 days after posting. Apply soon.
At a glance
- Experience2+ years
- Skills and toolsGoogle Cloud, Microsoft Office
Read from the ad by RoleFinder rules; the description is the source.
Back from the application? Add your CV and RoleFinder scores your fit for this role, then ranks your best 12 open roles where you want to work, each with a one-line reason.
Check my fitAbout the role
Job Overview
IQVIA is seeking an experienced Senior Clinical Trial Assistant | 2+ Years Experience Required to support the delivery of clinical research projects within a dynamic and collaborative environment.
Working closely with cross-functional study teams, you will contribute to the coordination, maintenance, and oversight of essential clinical trial documentation and processes, ensuring compliance with regulatory requirements and project timelines.
Essential Functions
- Support the management and maintenance of study documentation and tracking systems.
- Ensure accuracy, completeness, and quality of clinical trial records throughout the study lifecycle.
- Collaborate with clinical operations teams to coordinate study-related activities and communications.
- Assist with document preparation, filing, archiving, and quality control activities.
- Contribute to compliance with applicable regulatory requirements, SOPs, and Good Clinical Practice (GCP).
- Provide guidance and support to junior team members when appropriate.
- Participate in process improvement initiatives aimed at enhancing operational efficiency.
Qualifications
- Previous experience in a Clinical Trial Assistant, Clinical Research Coordinator, Study Coordinator, or similar clinical research support role.
- Minimum 2 years of experience within clinical research.
- Solid organizational and document management skills.
- Strong attention to detail and ability to manage multiple priorities.
- Excellent communication skills in Dutch/French and English.
- Good knowledge of Microsoft Office applications.
- Understanding of ICH-GCP and clinical research processes.
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
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.
Get open roles ranked against your CV
Add your CV once. RoleFinder ranks the open roles where you want to work, plus remote ones, against it, shows your best 12 with a one-line reason each, and emails you new matches once a week. The file is read once by AI and not kept; employers never see it.
Sign in with Google or email to start. How we handle your CV