Netherlands-Based Clinical Trial Assistant — Drive Study Execution

IQVIA Argentina

Amsterdam

On-site

EUR 38,000 - 52,000

Full time

5 days ago
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Job summary

IQVIA in the Netherlands is seeking a Clinical Trial Assistant to support CRAs and RSU within our CTAs-driven, full-service model. You will help maintain clinical systems, manage trial documentation, and assist with trial supplies and data flow, while coordinating communications across the clinical team.

The ideal candidate has 1 year CTA experience, fluent English and Dutch, and strong MS Office skills. Regular travel to Breda is required; the role offers professional development and a

Qualifications

  • CTA experience (1 year)
  • Fluent in English and Dutch
  • Knowledge of GCP/ICH guidelines
  • Proficient with MS Word, Excel and PowerPoint
  • Strong time management and organizational skills
  • Ability to build effective working relationships with team members and clients
  • Willingness to travel regularly to the Breda office (approx. two days/week)

Responsibilities

  • Assist CRAs/iCRA and RSU with updating and maintaining clinical systems to track site compliance and timelines
  • Handle clinical documentation and reports according to SOPs; assist with study file reviews
  • Assist with Clinical Trial Supplies tracking and documentation
  • Manage Case Report Forms, data queries, and data flow
  • Serve as central contact for project communications
  • Possibly accompany CRAs on site visits for monitoring duties
  • Support team with general administrative tasks for trial execution

Skills

CTA experience
English and Dutch fluency
GCP/ICH knowledge
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Time management
Interpersonal skills

Tools

Microsoft Word
Microsoft Excel
Microsoft PowerPoint

Job description

IQVIA in the Netherlands is seeking a Clinical Trial Assistant to support CRAs and RSU within our CTAs-driven, full-service model. You will help maintain clinical systems, manage trial documentation, and assist with trial supplies and data flow, while coordinating communications across the clinical team.

The ideal candidate has 1 year CTA experience, fluent English and Dutch, and strong MS Office skills. Regular travel to Breda is required; the role offers professional development and a

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