Clinical Research Assistant: Study Coordination & Compliance

Bon Secours Mercy Health; Toledo (OH); On-site; USD 52,000 - 78,000; Full time

Job summary

Bon Secours Mercy Health is seeking a Research Coordinator to oversee multi-site clinical research projects, including participant recruitment, data management, and regulatory compliance. You will prepare IRB documents, assist with grant applications, and liaise with investigators and sponsors to ensure studies adhere to all federal guidelines.

The role requires strong regulatory knowledge, collaboration with cross-functional teams, and the ability to manage multiple projects while maintaining

Responsibilities

• Coordinate research projects across MHSVMC and BSMH facilities.
• Recruit and monitor study participants.
• Maintain regulatory documents and ensure protocol compliance under federal/ICH-GCP guidelines.
• Prepare IRB-related documents and annual reports.
• Manage data, database prep, entry, and queries; assist with budget and grant applications.
• Liaise with investigators, sponsors, and regulatory bodies to communicate study needs.

Job description

Bon Secours Mercy Health is seeking a Research Coordinator to oversee multi-site clinical research projects, including participant recruitment, data management, and regulatory compliance. You will prepare IRB documents, assist with grant applications, and liaise with investigators and sponsors to ensure studies adhere to all federal guidelines.

The role requires strong regulatory knowledge, collaboration with cross-functional teams, and the ability to manage multiple projects while maintaining