Clinical Research Associate - Fsp

Parexel

Buenos Aires, Argentina
Fully remote
1 year monitoring experience
Knowledge of ich gcp
Data integrity and quality
At Parexel, we share the goal of improving the world's health through clinical trials and regulatory consulting

Job Summary

  • At Parexel, we share the goal of improving the world's health through clinical trials and regulatory consulting.
  • The Clinical Research Associate will ensure compliance with protocols and data integrity at clinical sites.
  • We are committed to building collaborative relationships and maintaining a high-performance culture.

Matching Summary

At Parexel, we share the goal of improving the world's health through clinical trials and regulatory consulting.

Skills & Requirements

Must-have

  • 1 year monitoring experience
  • knowledge of ICH GCP
  • data integrity and quality

Nice-to-have

  • client focused approach
  • strong analytical skills
  • flexible attitude towards work

Key Requirements

  • minimum 1 year as a clinical monitor
  • degree in biological science or related field
  • proficiency in English

Work Rights

Not specified

Tailored Resume

Cover Letter