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
Required Qualifications
- Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related discipline.
Preferred Qualifications
- SOCRA or ACRP certification.
- IATA certification.
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!