Research Study Coordinator II - Cancer Clinical Research

Our take on this role

About this role

Coordinate cancer research projects within regulatory guidelines, oversee recruitment, and manage day-to-day study operations. Direct contact with potential and enrolled study participants is expected.

What could you bring from clinical work?

• Nurses and PTs: Your experience following standardized protocols and maintaining accurate clinical records could help you coordinate research projects within regulatory guidelines.
• OTs and SLPs: Explaining assessment or participation requirements to patients and families may help you communicate with potential and enrolled study participants.
• Social workers: If you've explained services and helped people navigate participation barriers, that experience could support study recruitment and contact with potential participants.

Full job description from Henry Ford Health

Company Description
At Henry Ford Health, we're committed to advancing health and improving lives for the millions of people we serve across Michigan and around the world. As one of the nation's leading academic health systems, we provide a comprehensive continuum of care that includes primary and preventive services, specialty and complex care, virtual care, pharmacy, home health, eye care, health insurance, and more. With 12 hospitals and hundreds of ambulatory care locations, including former Ascension Southeast Michigan and Flint Region facilities, our growing network expands access to exceptional care in the communities we serve.

Headquartered in Detroit, Henry Ford Health is helping shape the future of healthcare through the transformative Future of Health: Detroit initiative, a $3 billion investment that is redefining our academic healthcare campus and advancing innovation, research, education, and community impact.

Our work is grounded in purpose, collaboration, and belonging. We empower team members to grow their careers, contribute innovative ideas, and make a meaningful difference every day. Whether you're caring for patients, supporting operations, conducting research, or driving new solutions, you'll be part of a team united by a shared mission: delivering exceptional care, advancing health outcomes, and building healthier communities for all.

Job Description
GENERAL SUMMARY:
Under minimal supervision the Research Study Coordinator II:
Coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation.
Provides technical support to Principal Investigators.
Duties include but not limited to:
Interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study.
Direct contact with potential and enrolled study participants expected.
Provides other support as required.
May work on multiple studies at any given time.

Qualifications
EXPERIENCE REQUIRED:
Bachelor’s degree in a scientific field, Psychology, Sociology, Anthropology, or related field.

One (1) year of research project coordination experience.
CERTIFICATIONS/LICENSURES REQUIRED:
SOCRA or ACRP and IATA certification preferred.

Job Type: Full Time