Clinical Research Coordinator - Onsite with Remote Options

Tekton Research; New Carlisle (OH); On-site; USD 55,000 - 85,000; Full time

Job summary

Tekton Research in New Carlisle, Ohio is seeking a Clinical Research Coordinator (Full-Time/Non-Exempt) to manage day-to-day coordination of Phase I–IV trials. The CRC will liaise with sponsors, CROs, investigators, study participants, and vendors, ensuring compliance with sponsor protocols, SOPs, ICH-GCP, FDA regulations, and IRB requirements.

The CRC will handle IP management when needed, ensure timely data capture, source documentation, and maintain regulatory files and logs.

Qualifications

• Experience leading clinical studies preferred (3-5 studies).
• Ability to work independently and as part of a team.

Responsibilities

• Coordinate day-to-day management of Phase I–IV trials.
• Maintain regulatory binders, ISF, logs and study documentation.
• Communicate with sponsors, CROs, investigators, and site staff.
• Assist with IP handling, source data entry, and adherence to GCP/FDA requirements.

Skills

Study coordination

Independent work

Education

High school diploma

Health science degree preferred

Job description

Tekton Research in New Carlisle, Ohio is seeking a Clinical Research Coordinator (Full-Time/Non-Exempt) to manage day-to-day coordination of Phase I–IV trials. The CRC will liaise with sponsors, CROs, investigators, study participants, and vendors, ensuring compliance with sponsor protocols, SOPs, ICH-GCP, FDA regulations, and IRB requirements.

The CRC will handle IP management when needed, ensure timely data capture, source documentation, and maintain regulatory files and logs.