# Senior Clinical Trial Assistant | 2+ Years Experience Required

**Company**: IQVIA
**Location**: Brussels, Brussels-Capital Region
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Brussels-Brussels-Capital-Region-Belgium/Senior-Clinical-Trial-Assistant--Sponsor-Dedicated---Belgium_R1578696?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/senior-clinical-trial-assistant-2-plus-years-a579b903-a0f/

## Description

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 organisational 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.

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## Skills

### Required
- Dutch
- French
- English
- Microsoft Office applications
- ICH-GCP
- clinical research processes
- organisational skills
- document management

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Brussels-Brussels-Capital-Region-Belgium/Senior-Clinical-Trial-Assistant--Sponsor-Dedicated---Belgium_R1578696?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)