Clinical Research Coordinator III

Henry Ford Health; Detroit (MI); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Career development opportunities

Mission-driven work environment

Collaborative team culture

Job summary

Henry Ford Health in Detroit seeks a Research Study Assistant III to support research projects under regulatory guidelines. You will interact with internal and external stakeholders, assist with day-to-day study operations, and help ensure protocol adherence.

The role focuses on contributing to low-to-moderate complexity studies, coordinating tasks, and engaging participants to enable successful research outcomes within a collaborative healthcare setting.

Qualifications

• High School Diploma or GED with 6 years of work experience including 4 years in research/healthcare.
• OR Bachelor's degree in a scientific field (Psychology, Sociology, Anthropology, or related).
• Preferred: experience with regulatory compliance in research settings.

Responsibilities

• Interact with internal and external customers to support research projects.
• Complete day-to-day operational tasks for assigned studies.
• Engage with potential and enrolled study participants to facilitate involvement.
• Analyze protocol-specific requirements and ensure stakeholder compliance.
• Coordinate low-to-moderate complexity research projects with timely completion.

Skills

Communication

Organizational skills

Regulatory compliance

Education

High School Diploma or GED

Bachelor's degree in a scientific field

Job description

Henry Ford Health in Detroit seeks a Research Study Assistant III to support research projects under regulatory guidelines. You will interact with internal and external stakeholders, assist with day-to-day study operations, and help ensure protocol adherence.

The role focuses on contributing to low-to-moderate complexity studies, coordinating tasks, and engaging participants to enable successful research outcomes within a collaborative healthcare setting.