Job Description

Job Overview:

The Senior Clinical Research Associate I monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines, ISO14155, and other applicable regulations. Builds, manages and supports strong site relationships while serving as liaison between the Sponsor and assigned sites.

Job Duties and Responsibilities:

  • Provides support to Project Team and Clinical Operations Team.
  • Maintains strong working knowledge of protocols and Monitoring Plans for assigned projects.
  • Demonstrates strong written and verbal communication skills.
  • Serves as primary contact for assigned research sites.
  • Verifies that the investigator, staff, and site facilities remain adequate throughout the trial period.
  • Responsible...

    • Ready to Apply?

    Take the next step in your AI career. Submit your application to Caidya today.

    Submit Application