Research Study Coordinator I- Individual & Genomic Medicine
Henry Ford Health · Detroit, Michigan
What the posting says
Each fact was read from this posting and checked:Statedin the posting, quotedConflictsposted two ways, both shownNot mentionedwe looked; it is not there
- Employment typeStated
- Full time
Not mentioned in this posting
We read the whole posting. These are not in it. Not a no: ask the recruiter, in your own words.
- PayNot mentioned
- The posting does not say
- Work arrangementNot mentioned
- The posting does not say
- ShiftNot mentioned
- The posting does not say
- ExperienceNot mentioned
- The posting does not say
- EducationNot mentioned
- The posting does not say
- Visa sponsorshipNot mentioned
- The posting does not say
Requirements, each with its sentence from the posting
These are the employer’s words. The index does not judge whether you meet them.
- No requirement has been itemized for this posting yet. The employer’s words are in the full posting below.
Read the full posting as the employer wrote it
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
Role Overview
As a Research Study Coordinator I, you will be responsible for coordinating research projects in strict adherence to regulatory compliance guidelines and federal regulations. You will provide essential technical support to Principal Investigators, manage participant recruitment, and oversee critical day-to-day study operations. Your work is essential to the successful execution of research studies and the integrity of scientific advancement.
Key Responsibilities
- Coordinate research projects in full compliance with regulatory requirements and Code of Federal Regulation guidelines.
- Provide technical support to Principal Investigators and research teams.
- Communicate with internal and external stakeholders at all organizational levels.
- Manage participant recruitment activities and oversee day-to-day study operations.
- Maintain direct communication with prospective and enrolled study participants.
- Execute additional responsibilities as required to maintain study integrity and compliance.
Qualifications
Qualifications
Required Qualifications
- Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related discipline.
Preferred Qualifications
- SOCRA or ACRP certification.
- IATA certification.
Additional Information
What We Offer
Join a team where you can grow your career, collaborate with experts, and contribute to mission-driven work. We provide opportunities for continuous learning and professional development in a supportive and innovative environment.
Join Our Team
Ready to make a difference? Apply now to become a Research Study Coordinator I at Henry Ford Health!
The posting text is reproduced as the employer wrote it; the index adds nothing to it.