Clinical Research Coordinator

Job Summary

A company is looking for a Clinical Research Coordinator, Sub-Studies.

Key Responsibilities

• Understand and interpret research protocols and manage required documentation
• Plan and execute sub-studies, including protocol writing and operational workflow design
• Monitor data collection and maintain collaborative relationships with investigational sites

Required Qualifications

• Bachelor's degree in a science discipline
• Minimum of two years of experience as a Research Associate or Research Coordinator
• Experience with Electronic Data Capture (EDC) systems
• CITI and/or CCRP certification is a plus
• Demonstrated ability to collaborate and manage multiple projects effectively