Research Study Coordinator I- Gastro Procedure
Henry Ford Health · Detroit, Michigan
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- Employment typeStated
- Full time
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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.
Job Description
About the Department
Join one of Michigan's largest physician organizations, delivering coordinated care across primary and specialty practices throughout the region. Henry Ford Medical Group offers collaborative teamwork, access to leading clinical resources, and opportunities to build lasting relationships with patients and communities. As part of this team, you'll contribute to innovative research that drives advancements in healthcare, making a meaningful impact on patient outcomes and medical knowledge.
Role Overview
As a Research Study Coordinator I, you will play a vital role in coordinating research projects under regulatory compliance guidelines. You'll 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 the advancement of medical science and patient care.
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 guidelines.
- Provide technical support to Principal Investigators.
- Oversee recruitment and day-to-day operations of research studies.
- Interact with internal and external stakeholders at all levels.
- Engage directly with potential and enrolled study participants.
Qualifications
What You Will Need
Required Qualifications
- Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related field.
- Must have reliable transportation.
Preferred Qualifications
- SOCRA or ACRP certification preferred.
- IATA certification preferred.
Additional Information
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, teamwork, and making a difference in healthcare.
Join Our Team
Ready to make an impact? Apply now and be part of our mission to advance healthcare through research and innovation.
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