Research Study Coordinator II- Dermatology
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 II, you will be responsible for coordinating research projects with minimal supervision while maintaining strict adherence to regulatory compliance guidelines. You will provide technical support to Principal Investigators, manage critical study operations, and maintain direct oversight of study participant interactions. Your performance will be essential to the integrity and success of medical research initiatives.
Key Responsibilities
- Coordinate research projects in full compliance with applicable regulatory guidelines and institutional policies.
- Provide technical support and guidance to Principal Investigators on study protocols and procedures.
- Oversee recruitment activities and manage all day-to-day operational requirements of assigned studies.
- Maintain professional interactions with internal and external stakeholders at all organizational levels.
- Manage direct contact with potential and enrolled study participants, ensuring accurate documentation and protocol adherence.
- Manage concurrent responsibilities across multiple studies while maintaining quality standards and regulatory compliance.
Qualifications
Required Qualifications
- Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related discipline.
- Minimum one (1) year of documented research project coordination experience.
Strongly Preferred Qualifications
- SOCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) certification.
- IATA (International Air Transport Association) certification or equivalent credential in research compliance.
Additional Information
What We Offer
At Henry Ford Health, we foster career growth through collaborative opportunities, mission-driven work, and continuous learning. Join a team where your contributions make a meaningful impact on healthcare and patient lives.
Join Our Team
Ready to make a difference? Apply now and be part of our mission to advance health and well-being in our communities.
The posting text is reproduced as the employer wrote it; the index adds nothing to it.