Research Study Assistant III- Sleep Medicine

  • Full-time
  • Job Type: Full Time

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

Job Title

Research Study Assistant III

Location: Novi, MI

 

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 your contributions directly impact the health and well-being of those we serve.

Role Overview

As a Research Study Assistant III, you will play a vital role in carrying out research projects within regulatory compliance guidelines. You¿ll interact with internal and external stakeholders, support study participants, and ensure adherence to protocol requirements. Your work will directly contribute to the success of low- to moderate-complexity research projects, driving meaningful outcomes for our patients and communities.

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

  • Interact with internal and external customers at all levels to support research study operations.
  • Engage directly with potential and enrolled study participants to ensure smooth study execution.
  • Analyze protocol-specific requirements and implement measures to ensure stakeholder compliance.
  • Coordinate low- to moderate-complexity research projects, ensuring adherence to regulatory guidelines.
  • Complete day-to-day operational tasks to support the success of research studies.

 

Qualifications

What You Will Need

Required Qualifications

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

Preferred Qualifications

  • Experience with regulatory compliance in research studies.
  • Strong interpersonal and communication skills for stakeholder engagement.

 

Additional Information

What We Offer

Join a team where you can grow your career, collaborate with dedicated professionals, and contribute to mission-driven work. We provide opportunities for continuous learning and development, empowering you to make a meaningful impact in healthcare.

Join Our Team

Ready to make a difference? Apply now and be part of our mission to advance health and wellness in our communities.

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