Clinical Research Coordinator III

Tekton Research

Clinical Research Coordinator managing clinical trials at Tekton Research. Overseeing daily operations and ensuring compliance with study protocols and regulations.

Posted 5/1/2026full-timeFort Collins • Colorado • 🇺🇸 United StatesMid-LevelSeniorWebsite

About the role

Key responsibilities & impact

Responsible for the overall management the studies assigned to you including administrative duties
Responsible for clear and direct communication with study sponsor, study monitor and CRO, PI and site manager
Manage the daily operations of assigned clinical trials.
Communicate with the investigator, sponsor and study participants all necessary information of the study.
Problem solve issues that may arise and to represent himself/herself and the site in the most professional, ethical and positive manner.
Inform study participants or caregivers about study procedures and outcomes to be expected
Train study team members and monitor study activities to ensure compliance with protocols

Requirements

What you’ll need

Experience leading 6-8 studies preferred
Ability to work independently and as a member of a team
GED or HS Diploma required (Some College preferred)
5+ years clinical research experience required

Benefits

Comp & perks

Health insurance
Competitive salary

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical researchstudy managementprotocol complianceproblem solvingtraining

Soft Skills

communicationindependenceteamworkprofessionalismethical conduct

Certifications

GEDHS DiplomaSome College