Clinical Research Coordinator

Job overview

The Clinical Research Coordinator role is a temporary, onsite position in Fort Collins, CO. Compensation is not specified. Tekton Research conducts clinical trials intended to advance medical knowledge and improve patient care. The coordinator manages assigned studies from start-up through close-out, supporting participant safety, data integrity, protocol compliance, and successful study execution. The role connects investigators, sponsors, participants, and regulatory agencies while maintaining study documentation and coordinating trial activities.

What you'll do

• Coordinate clinical trials from start-up through close-out
• recruit, screen, consent, and schedule participants
• process and ship specimens
• maintain source documentation and regulatory records
• monitor and report adverse events
• prepare IRB submissions and other regulatory documents
• collaborate with investigators, sponsors, monitors, and study staff
• assist with monitoring visits, audits, and inspections
• and use EDC and CTMS systems to maintain study data.

What we're looking for

Skills & competencies

clinical research coordinator

fort collins co

tekton research

temporary

onsite

clinical trials

good clinical practice

participant safety

irb submissions

specimen processing

edc

ctms

Work arrangement

• Weekend coverage required

Why this role

The posting identifies the position as temporary and onsite.

About the employer

Tekton Research Inc is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.