Site Research Assistant - Grenoble

IQVIA

Grenoble, France
Onsite
Clinical research study support
Maintain study documents and edc
Patient screening and enrollment support
The Site Research Assistant will support a clinical research study and maintain a safe study environment under the direction of the Principal Investigator

Job Summary

  • The Site Research Assistant will support a clinical research study and maintain a safe study environment under the direction of the Principal Investigator.
  • Responsibilities include maintaining study documents, supporting patient screening and enrollment, data entry, and managing biological samples.
  • The role requires a BS/BA in life sciences or equivalent experience, good knowledge of clinical trials, and at least 1-2 years of experience as a Clinical Research Assistant or Coordinator.

Matching Summary

The Site Research Assistant will support a clinical research study and maintain a safe study environment under the direction of the Principal Investigator.

Skills & Requirements

Must-have

  • Clinical research study support
  • Maintain study documents and EDC
  • Patient screening and enrollment support
  • Data entry and quality checking
  • Biological sample management
  • Fluent French language skills

Nice-to-have

  • Excellent interpersonal skills
  • Strong organizational skills
  • Attention to detail

Key Requirements

  • BS/BA in life sciences or educational equivalent
  • 1-2 years experience as Clinical Research Assistant/Coordinator
  • Basic medical terminology knowledge
  • Strong IT competence (MS Windows, Office)
  • Fluent French language skills

Work Rights

Not specified

Tailored Resume

Cover Letter