Impactful On-Site Clinical Research Coordinator (Temp)

Tekton Research; Fort Collins (CO); On-site; USD 39,000 - 55,000; Full time

Job summary

Tekton Research seeks a Clinical Research Coordinator (CRC) for a temporary, on-site role in Fort Collins, CO. The CRC will manage study start-up to close-out, coordinate enrollment, and oversee data integrity while ensuring GCP and FDA compliance.

Responsibilities include regulatory submissions (IRB), adverse event reporting, and collaboration with investigators and sponsors to ensure smooth trial conduct. Strong organizational and communication skills are essential.

Qualifications

• Bachelor’s degree in a related field preferred.
• Experience with GCP and FDA regulations is required or preferred.
• Experience coordinating multiple clinical studies and ensuring regulatory compliance.
• Experience with pediatric and adult sample handling is a plus.
• Strong organizational, time management, and communication skills.

Responsibilities

• Coordinate and manage all aspects of assigned clinical trials from start-up through close-out.
• Recruit, screen, consent, and schedule study participants per protocol.
• Prepare regulatory documents including IRB submissions and amendments.
• Maintain regulatory binders and source documents in GCP/FDA-compliant systems.
• Monitor participant safety and report adverse events promptly.
• Utilize EDC and CTMS to ensure accurate study data and documentation.

Skills

GCP knowledge

FDA regulations

Study coordination

EDC systems

CTMS usage

IRB submissions

Communication skills

Education

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

Tools

EDC systems

Microsoft Office

Job description

Tekton Research seeks a Clinical Research Coordinator (CRC) for a temporary, on-site role in Fort Collins, CO. The CRC will manage study start-up to close-out, coordinate enrollment, and oversee data integrity while ensuring GCP and FDA compliance.

Responsibilities include regulatory submissions (IRB), adverse event reporting, and collaboration with investigators and sponsors to ensure smooth trial conduct. Strong organizational and communication skills are essential.