Research Study Coordinator I: Clinical Trials & Participants

Henry Ford Health; Detroit (MI); On-site; USD 52,000 - 68,000; Full time

Job summary

Henry Ford Health is seeking a Research Study Coordinator I to coordinate research projects under regulatory guidelines and support Principal Investigators. You will manage day-to-day study operations and interact with study participants to ensure smooth execution and meaningful contributions to medical science.

The role requires collaboration with diverse teams, engagement with stakeholders, and a commitment to high-quality patient care in a leading academic healthcare system.

Qualifications

• Bachelor's degree in a scientific field (Psychology, Sociology, Anthropology, or related field).
• Must have reliable transportation.
• SOCRA or ACRP certification preferred.
• IATA certification preferred.

Responsibilities

• Coordinate research projects within regulatory compliance guidelines.
• Provide technical support to Principal Investigators.
• Oversee recruitment and day-to-day operations of research studies.
• Interact with internal and external stakeholders at all levels.
• Engage directly with potential and enrolled study participants.

Skills

Coordination

Education

Bachelor's degree in a scientific field

Job description

Henry Ford Health is seeking a Research Study Coordinator I to coordinate research projects under regulatory guidelines and support Principal Investigators. You will manage day-to-day study operations and interact with study participants to ensure smooth execution and meaningful contributions to medical science.

The role requires collaboration with diverse teams, engagement with stakeholders, and a commitment to high-quality patient care in a leading academic healthcare system.