Research Study Coordinator I- Cardiovascular Medicine

Job Description

Job Description

Company Description

Henry Ford Health partners with millions of people on their health journey, across Michigan and around the world. We offer a full continuum of services from primary and preventative care to complex and specialty care, health insurance, a full suite of home health offerings, virtual care, pharmacy, eye care and other health care retail. With former Ascension southeast Michigan and Flint region locations now part of our team, Henry Ford's care is available in 13 hospitals and hundreds of ambulatory care locations. Based in Detroit, Henry Ford is one of the nation's most respected academic medical centers and is leading the Future of Health: Detroit, a $3 billion investment anchored by a reimagined Henry Ford academic healthcare campus.

About the Department

Join Henry Ford Medical Group, one of Michigan's largest physician organizations, where we deliver 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 group that is dedicated to advancing healthcare through innovative research and patient-centered care.

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, manage day-to-day study operations, and interact directly with study participants. Your work ensures the smooth execution of research studies, contributing to advancements in healthcare and patient outcomes.

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.
• Engage directly with potential and enrolled study participants.
• Provide additional support as required to ensure study success.

Required Qualifications

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

Preferred Qualifications

• SOCRA or ACRP certification preferred.
• IATA certification preferred.

What We Offer

Join a team where you can grow your career through collaboration, mission-driven work, and continuous learning opportunities. Be part of an organization that values innovation, patient care, and professional development.

Join Our Team

Ready to make a difference? Apply now and be part of our mission to advance healthcare through research and exceptional care.