Clinical Research Associate I/ Clinical Research Associate Ii

Precision for Medicine

Paris, France
Remote
Ich-gcp compliance
Protocol adherence
Site monitoring
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards

Job Summary

  • You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
  • We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.
  • You will have a lower than average number of protocols, setting you up to be a protocol expert.

Matching Summary

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • protocol adherence
  • site monitoring
  • investigator identification
  • regulatory submissions

Nice-to-have

  • calm and thoughtful demeanor
  • creative problem-solving
  • client-focused approach
  • team player

Key Requirements

  • Life science degree or equivalent experience
  • 1 year or more CRA experience
  • Oncology study experience
  • Fluency in English and local language

Work Rights

Not specified

Tailored Resume

Cover Letter