Clinical Research Study Coordinator

Henry Ford Health; Novi (MI); On-site; USD 52,000 - 72,000; Full time

Job summary

Henry Ford Health in Michigan is seeking a research assistant under limited supervision to carry out projects within CFR guidelines. You will interact with internal and external customers and manage day-to-day study tasks.

You will coordinate with study participants, analyze protocol requirements for compliance, and may coordinate low-to-moderate complexity projects, with additional support as needed.

Qualifications

• High School Diploma or G.E.D. equivalent.
• Six (6) years of work experience, including at least four (4) years in research and/or healthcare.
• Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology or related field.

Responsibilities

• Carry out research projects under regulatory compliance and CFR guidelines.
• Interact with internal and external customers at all levels and perform day-to-day study tasks.
• Direct contact with potential and enrolled study participants.
• Analyze protocol requirements and ensure stakeholder compliance.
• Coordinate low- to moderate-complexity research projects.
• Provide other support as required.

Education

High School Diploma or G.E.D. equivalent

Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology or related field

Job description

Henry Ford Health in Michigan is seeking a research assistant under limited supervision to carry out projects within CFR guidelines. You will interact with internal and external customers and manage day-to-day study tasks.

You will coordinate with study participants, analyze protocol requirements for compliance, and may coordinate low-to-moderate complexity projects, with additional support as needed.