Clinical Research Coordinator - Drive Trial Excellence

Tekton Research Inc; New Carlisle (OH); On-site; USD 52,000 - 68,000; Full time

Job summary

Tekton Research in New Carlisle, OH seeks a Clinical Research Coordinator (CRC) to manage day-to-day coordination of clinical trials, ensure GCP compliance, recruit and screen participants, and maintain regulatory documentation.

The ideal candidate has 6 months to 1 year of CRC experience, knowledge of GCP/FDA guidelines, strong organizational skills, and the ability to work independently as part of a multidisciplinary team. A Bachelor's degree in a life science is preferred.

Qualifications

• High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred.
• Minimum of six months to one year of Clinical Research Coordinator experience.
• Working knowledge of GCP, FDA regulations, ICH guidelines, and clinical research processes.
• Experience with pediatric and adult phlebotomy and specimen processing.
• Proficiency with EDC systems and Microsoft Office applications.

Responsibilities

• Coordinate and manage all aspects of assigned clinical trials from start-up through close-out.
• Recruit, screen, consent, and schedule study participants according to protocol requirements.
• Collect, process, package, and ship laboratory specimens according to protocol and sponsor requirements.
• Maintain source documentation, regulatory binders, and study records in compliance with GCP, FDA regulations, and policies.
• Monitor participant safety and report adverse events.

Skills

Organizational skills

Time management

Communication skills

Independent work

Team collaboration

Multitasking

Education

Bachelor's degree in Nursing/Biology/Health Sciences/Public Health

Tools

Electronic Data Capture (EDC) systems

Microsoft Office

Job description

Tekton Research in New Carlisle, OH seeks a Clinical Research Coordinator (CRC) to manage day-to-day coordination of clinical trials, ensure GCP compliance, recruit and screen participants, and maintain regulatory documentation.

The ideal candidate has 6 months to 1 year of CRC experience, knowledge of GCP/FDA guidelines, strong organizational skills, and the ability to work independently as part of a multidisciplinary team. A Bachelor's degree in a life science is preferred.