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.