Clinical Research Assistant II — Onsite Studies

Henry Ford Health; Detroit (MI); On-site; USD 42,000 - 54,000; Full time

Job summary

Henry Ford Health in Detroit is seeking a Research Study Assistant II to support regulatory-compliant research projects across our medical group. You will interact with internal and external stakeholders, perform daily study tasks, and assist enrolled participants in a clinical setting.

The role requires at least a High School diploma (or GED) with three years in research/healthcare, or an Associates degree with one year of related experience.

Qualifications

• Experience with regulatory compliance in research settings.
• Strong organizational and communication skills.

Responsibilities

• Interact with internal and external customers at all levels to support research projects.
• Complete day-to-day operational tasks for ongoing studies.
• Engage directly with potential and enrolled study participants.
• Analyze protocol-specific requirements and implement measures to ensure stakeholder compliance.
• Provide additional support as required to meet project goals.

Skills

Stakeholder communication

Regulatory compliance

Data entry

Education

High School Diploma or GED

Associates degree

Job description

Henry Ford Health in Detroit is seeking a Research Study Assistant II to support regulatory-compliant research projects across our medical group. You will interact with internal and external stakeholders, perform daily study tasks, and assist enrolled participants in a clinical setting.

The role requires at least a High School diploma (or GED) with three years in research/healthcare, or an Associates degree with one year of related experience.