Temporary Clinical Research Coordinator

Job overview

The Temporary Clinical Research Coordinator role is onsite in Longmont, 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, protocol compliance, reliable study data, and successful trial execution. The role connects investigators, sponsors, participants, and regulatory agencies.

What you'll do

• Coordinate clinical trials from start-up through close-out
• recruit, screen, consent, and schedule participants
• collect and process specimens
• maintain source documentation and regulatory records
• monitor and report adverse events
• prepare IRB submissions and amendments
• assist with monitoring visits, audits, and inspections
• use EDC and CTMS systems.

What we're looking for

Skills & competencies

temporary

clinical research coordinator

clinical trials

gcp

participant safety

phlebotomy

specimen processing

regulatory documentation

edc systems

ctms

longmont co

tekton research

Work arrangement

• Weekend coverage required

Benefits & perks

• Posting mentions competitive compensation, comprehensive benefits, and professional growth opportunities.

Why this role

Temporary, onsite clinical research role requiring GCP knowledge and pediatric and adult phlebotomy and specimen-processing experience.

About the employer

Tekton Research Inc is hiring for this role. Industry: Research and Development in Biotechnology (except Nanobiotechnology). Sector: 54.