Site Research Assistant - Nijmegen

IQVIA

Nijmegen, Netherlands
Onsite
Study documentation maintenance
Clinical trial logistics coordination
Data entry and quality checks
You will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks

Job Summary

  • You will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks.
  • Key responsibilities include maintaining study documentation, coordinating logistical activities, performing data entry, and assisting with patient recruitment.
  • At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science.

Matching Summary

You will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks.

Skills & Requirements

Must-have

  • study documentation maintenance
  • clinical trial logistics coordination
  • data entry and quality checks
  • patient recruitment assistance
  • MS Office proficiency

Nice-to-have

  • interpersonal and communication skills
  • organizational skills and attention to detail
  • advancing healthcare through data

Key Requirements

  • Bachelor's degree or equivalent experience
  • 1-2 years experience as CRA, RN, or CRC
  • Fluency in Dutch and English

Work Rights

Not specified

Tailored Resume

Cover Letter