Research Study Coordinator I Center for Individual Genomic Medicine

Henry Ford Health; Detroit (MI); On-site; USD 42,000 - 64,000; Full time

Job summary

Henry Ford Health in Detroit is seeking a Research Study Coordinator I to support clinical research across departments. You will coordinate studies, ensure regulatory compliance, and provide technical support to Principal Investigators to help advance patient care and scientific discovery.

You will oversee recruitment and day-to-day study operations, maintain contact with potential and enrolled participants, and collaborate with internal and external stakeholders to drive study success.

Qualifications

• Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related field.
• Phlebotomy experience or certification (preferred).
• SOCRA or ACRP certification (preferred).
• IATA certification (preferred).

Responsibilities

• Coordinate research projects within regulatory compliance and Code of Federal Regulation guidelines.
• Provide technical support to Principal Investigators.
• Interact with internal and external stakeholders at all levels.
• Oversee recruitment and manage day-to-day operations of the study.
• Maintain direct contact with potential and enrolled study participants.
• Provide additional support as required to ensure study success.

Education

Bachelor's degree in a scientific field

Job description

Job Description

Research Study Coordinator I - Henry Ford Health

Job Title

Research Study Coordinator I

About the Department

Join Henry Ford Medical Group, one of Michigan's largest physician organizations, dedicated to delivering coordinated care across primary and specialty practices throughout the region. Our team thrives on collaborative teamwork, access to leading clinical resources, and the opportunity to build lasting relationships with patients and communities. Be part of a dynamic environment where innovation and patient-centered care are at the forefront of everything we do.

Role Overview

As a Research Study Coordinator I, you will play a vital role in coordinating research projects within regulatory compliance guidelines. You will provide technical support to Principal Investigators, oversee recruitment, and manage day-to-day study operations. Your work ensures the smooth execution of research studies, directly impacting patient care and scientific advancement.

Why Henry Ford Health

At Henry Ford Health, we are relentless advocates for exceptional care for our patients, communities, and each other. We come to do meaningful work and grow our careers, and we stay for the connection, support, and shared pride in making the impossible, possible.

What You Will Do

• Coordinate research projects within regulatory compliance and Code of Federal Regulation guidelines.
• Provide technical support to Principal Investigators.
• Interact with internal and external stakeholders at all levels.
• Oversee recruitment and manage day-to-day operations of the study.
• Maintain direct contact with potential and enrolled study participants.
• Provide additional support as required to ensure study success.

What You Will Need

Required Qualifications

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

Preferred Qualifications

• Phlebotomy Experience or Certification
• SOCRA or ACRP certification preferred.
• IATA certification preferred.

What We Offer

Join a team where you can grow your career, collaborate with experts, and contribute to mission-driven work. We provide opportunities for continuous learning and professional development in a supportive and innovative environment.