Clinical Trial Assistant — Multisite Support (Netherlands)

IQVIA; Amsterdam; On-site; EUR 36,000 - 51,000; Full time

Job summary

IQVIA in Amsterdam, Netherlands, is seeking a Clinical Trial Assistant (CTA) to support clinical teams within our global, full-service model. This full-time role involves working closely with CRAs/iCRA and RSU, updating systems, and ensuring documentation meets GCP/ICH standards.

Based in the Netherlands with regular travel to our Breda office (roughly two days per week), you will use MS Word/Excel/PowerPoint and communicate effectively in English and Dutch to keep studies on track and compliant.

Qualifications

• 1 year of CTA experience.
• Fluent written and spoken English and Dutch.
• Strong communication skills.
• Good time management and organizational abilities.
• Able to collaborate with cross-functional teams.

Responsibilities

• Assist CRAs/iCRA and RSU with updating clinical systems tracking site compliance and timelines.
• Assist with preparation, handling, distribution, filing and archiving of clinical documents per SOPs.
• Assist with tracking CRFs, queries and data flow.
• Support distribution of Clinical Trial Supplies and tracking information.
• Serve as central contact for project communications and documentation.

Skills

CTA experience

English and Dutch fluency

Communication

Time management

Organizational skills

Teamwork

Tools

MS Word

MS Excel

MS PowerPoint

Job description

IQVIA in Amsterdam, Netherlands, is seeking a Clinical Trial Assistant (CTA) to support clinical teams within our global, full-service model. This full-time role involves working closely with CRAs/iCRA and RSU, updating systems, and ensuring documentation meets GCP/ICH standards.

Based in the Netherlands with regular travel to our Breda office (roughly two days per week), you will use MS Word/Excel/PowerPoint and communicate effectively in English and Dutch to keep studies on track and compliant.