On-Site Temporary Clinical Research Coordinator

Tekton Research Inc; Fort Collins (CO); On-site; USD 48,000 - 58,000; Full time

Job summary

Tekton Research Inc. in Fort Collins, CO, is seeking a temporary Clinical Research Coordinator to oversee day-to-day trial coordination on-site.

This role supports multiple studies, ensures GCP compliance, and acts as a liaison among investigators, sponsors, participants, and regulatory bodies. The CRC will manage start-up through close-out, recruit and screen participants, handle specimen processing, maintain study records, monitor safety, and prepare regulatory submissions.

Qualifications

• High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, or related field preferred.
• Minimum of six months to one (1) year of Clinical Research Coordinator experience.
• Working knowledge of GCP, FDA regulations, ICH guidelines, and clinical research processes.

Responsibilities

• Coordinate and manage all aspects of assigned clinical trials from study 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 accurate source documentation, regulatory binders, and study records in compliance with GCP, FDA regulations, and institutional policies.
• Monitor participant safety and promptly identify, document, and report adverse events.
• Prepare and submit regulatory documents, including IRB submissions, continuing reviews, and protocol amendments.
• Collaborate with investigators, sponsors, monitors, and study staff to ensure successful study conduct.
• Assist with monitoring visits, sponsor audits, and regulatory inspections.
• Utilize EDC systems and CTMS to maintain accurate study data.
• Ensure protocol compliance while maintaining the highest standards of participant care and research integrity.

Skills

GCP knowledge

FDA regulations

Clinical research coordination

Education

Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or related field

Job description

Tekton Research Inc. in Fort Collins, CO, is seeking a temporary Clinical Research Coordinator to oversee day-to-day trial coordination on-site.

This role supports multiple studies, ensures GCP compliance, and acts as a liaison among investigators, sponsors, participants, and regulatory bodies. The CRC will manage start-up through close-out, recruit and screen participants, handle specimen processing, maintain study records, monitor safety, and prepare regulatory submissions.