Clinical Research Coordinator II: Study Ops & Compliance

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

Job summary

Henry Ford Health in Michigan seeks a Research Study Coordinator II to coordinate research projects under minimal supervision, ensuring regulatory compliance and timely study operations. You will support Principal Investigators, manage day-to-day activities, recruit participants, and interact with internal and external stakeholders to advance healthcare research.

Bachelor’s degree in a scientific field and at least one year of coordination experience are required; certifications in SOCRA/ACRP

Qualifications

• Bachelor's degree in a scientific field (e.g., Psychology, Sociology, Anthropology, or related).
• At least 1 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.

Skills

Research coordination

Regulatory compliance

Stakeholder communication

Multi-study management

Education

Bachelor's in science field

Tools

SOCRA certification

ACRP certification

IATA certification

Job description

Henry Ford Health in Michigan seeks a Research Study Coordinator II to coordinate research projects under minimal supervision, ensuring regulatory compliance and timely study operations. You will support Principal Investigators, manage day-to-day activities, recruit participants, and interact with internal and external stakeholders to advance healthcare research.

Bachelor’s degree in a scientific field and at least one year of coordination experience are required; certifications in SOCRA/ACRP