# Senior Clinical Trial Assistant

**Company**: IQVIA
**Location**: Amsterdam
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/Senior-Clinical-Trial-Assistant---Sponsor-dedicated---Netherlands--Hybrid--m-w-d-_R1578777?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/senior-clinical-trial-assistant-1467e2d8-4ad/

## Description

At IQVIA, our Clinical Functional Service Partnership (CFSP) model offers the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA.

As a Senior Clinical Trial Assistant within Clinical FSP, you'll work closely with cross-functional study teams, contributing to the coordination, maintenance, and oversight of essential clinical trial documentation and processes, ensuring compliance with regulatory requirements and project timelines.

**Key Responsibilities:**

- 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.

**Requirements:**

- 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 and English.

- Good knowledge of Microsoft Office applications.

- Understanding of ICH-GCP and clinical research processes.

If you're looking to build a career in clinical research and want to contribute to studies that improve patient outcomes worldwide, we would love to hear from you.

For more fresh new jobs, check out [yubhub.co](https://yubhub.co/).

## Skills

### Required
- Dutch
- English
- Microsoft Office applications
- ICH-GCP
- clinical research processes

---

Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/Senior-Clinical-Trial-Assistant---Sponsor-dedicated---Netherlands--Hybrid--m-w-d-_R1578777?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)