Clinical Research Coordinator I – Patient-Focused Studies

Henry Ford Health Care; Detroit (MI); On-site; USD 50,000 - 70,000; Full time

Job summary

Henry Ford Health is seeking a Research Study Coordinator I to support coordination of clinical studies within regulatory compliance guidelines. You will assist Principal Investigators, oversee recruitment, and manage day-to-day study operations to advance patient care and scientific progress.

You will work across departments to maintain study records, ensure data integrity, and support audits, trainings, and sponsor communications in a fast-paced environment.

Qualifications

• Bachelor's degree in a scientific discipline, Psychology, Sociology, Anthropology, Public Health, Healthcare Administration, or related field.
• Experience interacting directly with patients in clinical, research, or healthcare settings.
• Knowledge of human subjects research, including informed consent and regulatory requirements.
• Experience maintaining study documentation and regulatory binders.

Responsibilities

• Reviews study protocols, timelines, and project requirements.
• Maintains study databases, participant recruitment, specimen management, and supplies.
• Organizes study files, regulatory binders, and source documentation.
• Coordinates site visits, sponsor tours, and study meetings with compliance.
• Supports investigator meetings and communicates updates to stakeholders.
• Trains staff, develops materials, and supports recruitment plans.
• Keeps up with regulatory practices and new research guidelines.
• Communicates with sponsors to clarify protocol requirements.

Skills

Patient interaction

Communication skills

Regulatory knowledge

Education

Bachelor's degree in a scientific discipline or related field

Tools

Microsoft Office

Job description

Henry Ford Health is seeking a Research Study Coordinator I to support coordination of clinical studies within regulatory compliance guidelines. You will assist Principal Investigators, oversee recruitment, and manage day-to-day study operations to advance patient care and scientific progress.

You will work across departments to maintain study records, ensure data integrity, and support audits, trainings, and sponsor communications in a fast-paced environment.