Clinical Research Coordinator II – Emergency Medicine

Cincinnati Children's; Kasota (MN); On-site; USD 34,000 - 39,000; Full time

Job summary

Cincinnati Children’s seeks a dedicated Research Support Specialist to assist in coordinating clinical studies, preparing protocols, and ensuring regulatory compliance. You will help recruit participants, manage data, and maintain study documentation in a fast-paced emergency medicine setting.

Responsibilities include coordinating materials, obtaining informed consent, and supporting audits while maintaining accurate records and effective communication with the team and sponsors.

Qualifications

• High school diploma or equivalent.
• 2+ years of work experience in a related job discipline or equivalent combination of education and experience.
• May require an Associate degree, vocational training, apprenticeships or equivalent.

Responsibilities

• Study Conduct/ Clinical Research Practice - Assist in coordinating studies by preparing personnel and materials, preparation of protocols, informed consents, amendments and other necessary documents for review by the IRB and Sponsor.
• Regulatory Compliance and Documentation - Identify regulatory activities to be completed and takes the initiative to complete. Coordinate and participate in the assembly of materials.
• Recruitment/Enrollment/Retention - Maintain awareness of status of all active studies. Identify potentially eligible participants. Coordinate, plan and execute study visits and provide instructions and reimbursement to participants.
• Communication - Assist with organizing and filing all correspondence. Refer questions and issues that arise during study conduct to the appropriate research team member.
• Data Management - Complete Case Report Forms (CRFs) and source documentation in compliance with all applicable guidelines for human research.

Skills

Experience in related field

Regulatory awareness

Education

High school diploma or equivalent

Associate degree (preferred)

Job description

Cincinnati Children’s seeks a dedicated Research Support Specialist to assist in coordinating clinical studies, preparing protocols, and ensuring regulatory compliance. You will help recruit participants, manage data, and maintain study documentation in a fast-paced emergency medicine setting.

Responsibilities include coordinating materials, obtaining informed consent, and supporting audits while maintaining accurate records and effective communication with the team and sponsors.