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.
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.
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.