Clinical Research Coordinator II — Patient-Centric Trials

Henry Ford Health; Detroit (MI); On-site; USD 55,000 - 75,000; Full time

Job summary

Henry Ford Health is seeking a Research Study Coordinator II to manage day-to-day study operations, ensure regulatory compliance, and support Principal Investigators. The role entails direct interaction with study participants and collaboration with internal and external stakeholders within a large academic medical setting.

You will oversee recruitment, ensure study timelines are met, and coordinate across multiple studies while maintaining high data integrity and participant safety.

Qualifications

• Bachelor's degree in a scientific field (psychology, sociology, anthropology, or related field).
• One year of research project coordination experience.
• SOCRA or ACRP certification preferred.
• IATA certification preferred.

Responsibilities

• Coordinate research projects within regulatory compliance guidelines.
• Provide technical support to Principal Investigators.
• Interact with internal and external customers at all levels.
• Oversee recruitment and manage day-to-day operations of studies.
• Maintain direct contact with potential and enrolled study participants.
• Support multiple studies simultaneously as needed.

Education

Bachelor's degree in a scientific field

Job description

Henry Ford Health is seeking a Research Study Coordinator II to manage day-to-day study operations, ensure regulatory compliance, and support Principal Investigators. The role entails direct interaction with study participants and collaboration with internal and external stakeholders within a large academic medical setting.

You will oversee recruitment, ensure study timelines are met, and coordinate across multiple studies while maintaining high data integrity and participant safety.