Clinical Research Coordinator

Job Summary

The full-time Clinical Research Coordinator will manage and coordinate research activities for two International Rare Tumor Registries, ensuring compliance with study protocols while working in a hybrid environment.

Key responsibilities

• Organize and manage all aspects of assigned research activities, ensuring compliance with study protocols
• Prepare regulatory submissions and maintain compliance with federal and local agencies according to Good Clinical Practice guidelines
• Facilitate study-related communications and interact with patients and families for securing informed consent and data collection

Required qualifications

• Baccalaureate in a health-related field with at least four years of clinical research experience, or a registered nurse with two years of clinical research experience
• Master's degree in a related field with two years of clinical research experience is also acceptable
• Preferred experience working with children
• SoCRA or ACRP certification is preferred
• Detail-oriented with strong writing, communication, and computer skills