Research Study Coordinator I- Gynecologic Oncology
Company: Henry Ford Health
- Location: Royal Oak, United States
- Seniority: Entry level
- Employment type: Full-time
- Posted: Today
- Offer language: English
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.
Job Description
About the Department
Join one of Michigan's largest physician organizations, Henry Ford Medical Group, where we deliver coordinated care across primary and specialty practices throughout the region. Our team is dedicated to collaborative teamwork, providing access to leading clinical resources, and fostering lasting relationships with patients and communities. As part of Henry Ford Health, you'll contribute to a culture of innovation and excellence in healthcare research and patient care.
Role Overview
As a Research Study Coordinator I, you will play a vital role in coordinating research projects under minimal supervision, ensuring compliance with regulatory guidelines. You'll provide technical support to Principal Investigators, manage day-to-day study operations, and interact directly with study participants. Your work will directly support the advancement of medical research and improve 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 guidelines.
- Provide technical support to Principal Investigators.
- Interact with internal and external stakeholders at all levels.
- Oversee recruitment and manage day-to-day study operations.
- Engage directly with potential and enrolled study participants.
Qualifications
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.
Additional Information
What We Offer
Join a team where you can grow your career, collaborate with experts, and contribute to mission-driven work that makes a difference. We provide opportunities for continuous learning and professional development in a supportive and innovative environment.
Join Our Team
Ready to make an impact? Apply now and be part of our mission to advance healthcare through research and innovation.
