Research Study Coordinator I - Full Time Position in Research Administration

Overview

This role involves coordinating research projects with adherence to regulatory guidelines and the Code of Federal Regulations, operating under minimal supervision. The coordinator offers technical assistance to Principal Investigators and ensures smooth day-to-day management of studies, including recruitment and engagement with study participants.

Key Responsibilities

• Coordinate research projects ensuring compliance with relevant regulations.
• Provide technical support to Principal Investigators throughout clinical trials.
• Engage with both internal and external stakeholders at various organizational levels.
• Oversee recruitment processes and manage daily study operations.
• Maintain direct contact with potential and enrolled study participants.
• Perform additional duties as assigned.

Qualifications and Experience

• Bachelor’s degree in a scientific discipline such as Psychology, Sociology, Anthropology, or related fields.
• Certification or licensure in SOCRA or ACRP and IATA certification preferred.
• Clinical trial experience is mandatory with a strong preference for knowledge covering the full clinical research process.

Additional Details

• Organization: Henry Ford Medical Group
• Department: Clinical Trials Office Strategy
• Work Shift: Day job
• Union Status: Not Applicable