Site Research Assistant - Grenoble

IQVIA UK

Grenoble, France
Onsite
Maintain study documents
Patient screening and enrollment
Data entry and quality checking
The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies

Job Summary

  • The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies.
  • You will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies.

Skills & Requirements

Must-have

  • Maintain study documents
  • Patient screening and enrollment
  • Data entry and quality checking
  • Manage biological samples
  • Coordinate with study monitor
  • Fluent French language skills

Nice-to-have

  • Interpersonal skills
  • Organizational skills
  • Attention to detail

Key Requirements

  • BS/BA in life sciences or educational equivalent
  • 1-2 years experience as CRA or CRC
  • Good knowledge of clinical trials
  • Basic knowledge of medical terminology
  • Strong IT competence

Work Rights

Not specified

Tailored Resume

Cover Letter