Clinical Research Associate - Fsp

Parexel

São Paulo, Brazil
Fully remote
1 year monitoring experience
Knowledge of clinical trial methodologies
Ability to manage investigator site relationships
At Parexel, we all share the same goal - to improve the world's health

Job Summary

  • At Parexel, we all share the same goal - to improve the world's health.
  • The CRA is responsible for site management and monitoring to ensure patient safety and quality study execution.
  • We take our work personally, we do it with empathy and we're committed to making a difference.

Matching Summary

At Parexel, we all share the same goal - to improve the world's health.

Skills & Requirements

Must-have

  • 1 year monitoring experience
  • knowledge of clinical trial methodologies
  • ability to manage investigator site relationships

Nice-to-have

  • preferred therapeutic experience in Oncology
  • global clinical trial experience
  • effective verbal and written communication skills

Key Requirements

  • Bachelor’s degree in life sciences
  • fluent in English and native language
  • valid driver’s license and passport required

Work Rights

Not specified

Tailored Resume

Cover Letter