Clinical Research Associate

Job Summary

A company is looking for a FSP CRA (Level I/II).

Key Responsibilities

• Monitor investigator sites using a risk-based approach, ensuring compliance and data accuracy
• Document observations and communicate deficiencies to clinical management promptly
• Initiate clinical trial sites and conduct trial close-out activities as per regulatory requirements

Required Qualifications and Education

• Strong background in HSA and IRB submissions, with knowledge of ECOS
• Understanding of ICH-GCP and applicable regulations
• Experience in trial status tracking and progress reporting
• Ability to facilitate communication between investigative sites and project teams
• Proficiency in completing administrative tasks, such as expense reports and timesheets