Clinical Research Associate

13 hours ago

Shanghai, Shanghai, China Fortrea Full time
Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team at Fortrea. As a Clinical Research Associate, you will be responsible for monitoring study sites, ensuring compliance with regulatory requirements, and maintaining accurate records.

Key Responsibilities
  • Monitor study sites to ensure compliance with protocol and regulatory requirements
  • Conduct site initiation and close-out visits
  • Review and maintain accurate records of study data
  • Ensure timely and efficient completion of study tasks
  • Collaborate with vendors and other stakeholders to ensure smooth study execution
  • Perform other duties as assigned by management
Requirements
  • At least 1 year of clinical monitoring experience
  • Ability to work independently and as part of a team
  • Excellent communication and interpersonal skills
  • Strong analytical and problem-solving skills
  • Fluent in English, both written and verbal
  • Valid driver's license
Education/Qualifications/Certifications and Licenses
  • University or college degree in a related field
  • Thorough knowledge of ICH Guidelines and local regulatory requirements
  • Basic understanding of the clinical trial process
Why Join Fortrea?

Fortrea is an Equal Opportunity Employer committed to diversity and inclusion. We strive to create a workplace that is free from harassment and discrimination. We make employment decisions based on the needs of our business and the qualifications of the individual.

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