Clinical Research Coordinator - Onsite with Remote Options

Automatic Data Processing, Inc.; New Carlisle (OH); On-site; USD 52,000 - 76,000; Full time

Job summary

Tekton Research, located in New Carlisle, OH, is seeking a Clinical Research Coordinator (Full-Time/Non-Exempt) to manage day-to-day coordination of Phase I–IV trials. You will ensure compliance with sponsor protocols, ICH-GCP, FDA regulations, and IRB requirements.

The role involves participant recruitment, consent, scheduling, data capture, documentation, and collaboration with sponsors, CROs, investigators, and vendors, with on-site focus and occasional remote support as needed.

Qualifications

• 2+ years of clinical research experience preferred.
• Experience leading 3-5 studies preferred.
• Ability to work independently and as part of a team.

Responsibilities

• Coordinate day-to-day activities of Phase I–IV trials.
• Ensure regulatory, sponsor, and IRB compliance.
• Coordinate participant recruitment, informed consent, and visits.
• Maintain study documentation, ISF, and regulatory binders.
• Manage data entry and source documentation timelines.
• Monitor safety reporting requirements and QA audits.
• Communicate with sponsors, CROs, investigators, and vendors.
• Onsite clinical duties with occasional remote work as needed.

Skills

Clinical coordination

Communication

Teamwork

Education

High school diploma

Associate or Bachelor’s degree in health science

Job description

Tekton Research, located in New Carlisle, OH, is seeking a Clinical Research Coordinator (Full-Time/Non-Exempt) to manage day-to-day coordination of Phase I–IV trials. You will ensure compliance with sponsor protocols, ICH-GCP, FDA regulations, and IRB requirements.

The role involves participant recruitment, consent, scheduling, data capture, documentation, and collaboration with sponsors, CROs, investigators, and vendors, with on-site focus and occasional remote support as needed.