# Clinical Trial Assistant

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/Clinical-Trial-Assistant-2_R1571201?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_7fb9f534-344

## 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 Clinical Trial Assistant within Clinical FSP, you'll gain hands-on exposure to real study operations, build foundational expertise alongside experienced CRAs and Project Managers, and develop a clear path toward future clinical research roles, all within a global organization dedicated to transforming healthcare through human science and data science.

**Key Responsibilities:**

- Maintain and update Trial Master Files (TMF) and study documentation.

- Support document preparation, filing, tracking, and archiving.

- Review study files for completeness and compliance.

- Coordinate clinical trial supplies and tracking records.

- Assist with CRF tracking, study queries, and data workflows.

- Act as a key contact for project communications and documentation.

- Provide guidance and mentorship to Clinical Trial Assistants, supporting onboarding, training, and knowledge sharing across the team.

- Serve as a subject matter expert for clinical trial processes and may lead CTA study teams and contribute to recruitment activities.

- Support departmental quality and process improvement initiatives.

**What You'll Bring:**

- Regular travel to the Breda office is required, typically 1 day a week.

- Passion for clinical research and healthcare.

- Science degree preferred.

- Previous exposure to clinical research or clinical trials support is preferred.

- Good written and verbal communication skills including fluent command of English and Dutch language.

- Proficiency in Microsoft Office (Word, Excel, PowerPoint).

- Strong organisation skills and attention to detail.

- Ability to manage multiple priorities and meet deadlines.

- Effective communication skills with the ability to work collaboratively across teams.

## Skills

### Required
- Microsoft Office
- English
- Dutch
- clinical research
- organisation
- communication

### Nice to have
- science degree
- previous exposure to clinical research or clinical trials support

---

Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/Clinical-Trial-Assistant-2_R1571201?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)