Clinical Research Associate

Trzdev28

On-site monitoring experience
Knowledge in gcp clinical therapeutics
Ability to manage multiple tasks
The role involves initiating, organizing, and managing assigned studies

Job Summary

  • The role involves initiating, organizing, and managing assigned studies.
  • You will ensure compliance with clinical trial protocols and GCP.
  • The position requires solving complex problems across various studies.

Matching Summary

The role involves initiating, organizing, and managing assigned studies.

Skills & Requirements

Must-have

  • on-site monitoring experience
  • knowledge in GCP clinical therapeutics
  • ability to manage multiple tasks

Nice-to-have

  • good interpersonal skills
  • team player attitude
  • excellent command of English

Key Requirements

  • Bachelor's degree in pharmacy or health science
  • at least 2 years of CRA experience
  • excellent written and spoken English

Work Rights

Not specified

Tailored Resume

Cover Letter