Clinical Research Coordinator — Drive Phase I–IV Trials

CTI Clinical Trial and Consulting Services; Cincinnati (OH); Hybrid; USD 55,000 - 75,000; Full time

Benefits offered by this job

Hybrid work from home opportunities

Health benefits

Vacation packages

Paid parental leave

CTI Cares program

Job summary

CTI Clinical Trial and Consulting Services in Cincinnati seeks a Clinical Research Coordinator to coordinate Phase I through IV studies in line with GCPs, ICH guidelines, and SOPs, from pre-study planning to the final study visit. You’ll recruit volunteers, prepare study templates, and ensure protocol compliance while maintaining participant safety.

You will interact with investigators and sponsor monitors, contribute to data quality, and seek professional development opportunities within a

Qualifications

• 1+ year of experience as a clinical research coordinator or in a similar position.
• Bachelor’s degree in life sciences or related field.
• CCRC certification preferred; nursing degrees preferred.
• ACLS preferred.

Responsibilities

• Coordinate conduct of multicenter clinical research studies per GCPs and SOPs from planning to completion.
• Recruit volunteers and assist with materials and interview questionnaires.
• Create study documents, complete case report forms, and ensure protocol compliance.
• Maintain subject safety and manage medication administration per licensure.
• Coordinate and conduct study visits and communicate with investigators and sponsors.

Skills

Clinical research coordination

Informed consent

Study visit coordination

Communication skills

Education

Bachelor's degree in life sciences or related field

Associate or Bachelor’s Degree in Nursing is preferred

Clinical Research Coordinator Certification (CCRC) is preferred

Job description

CTI Clinical Trial and Consulting Services in Cincinnati seeks a Clinical Research Coordinator to coordinate Phase I through IV studies in line with GCPs, ICH guidelines, and SOPs, from pre-study planning to the final study visit. You’ll recruit volunteers, prepare study templates, and ensure protocol compliance while maintaining participant safety.

You will interact with investigators and sponsor monitors, contribute to data quality, and seek professional development opportunities within a