Clinical Research Associate Sr

Zse68

3 to 5 years of cra experience
Clinical monitoring visits
Knowledge of good clinical practices
The CRA is responsible for delivering studies at assigned sites

Job Summary

  • The CRA is responsible for delivering studies at assigned sites.
  • They act as the primary contact with the study site to ensure proper study execution.
  • The role involves monitoring study performance and contributing to investigator meetings.

Matching Summary

The CRA is responsible for delivering studies at assigned sites.

Skills & Requirements

Must-have

  • 3 to 5 years of CRA experience
  • Clinical monitoring visits
  • Knowledge of Good Clinical Practices

Nice-to-have

  • Ability to train and support investigators
  • Strong collaboration skills
  • Commitment to patient welfare

Key Requirements

  • University degree in health-related field
  • Clinical research monitoring course required
  • Advanced English language skills

Work Rights

Not specified

Tailored Resume

Cover Letter