Senior Clinical Research Coordinator – Fort Collins, CO (on-site)
Tekton Research is seeking an experienced Senior Clinical Research Coordinator (CRC III) to oversee the day-to-day management of multiple clinical trials while ensuring compliance with study protocols, regulatory requirements, and site SOPs. In this role, you will serve as the primary liaison between sponsors, CROs, investigators, and study participants, coordinating all aspects of study execution from participant visits and data entry to drug accountability, regulatory documentation, monitoring visits, and quality audits. The ideal candidate has at least five years of clinical research experience, experience managing multiple studies, strong organizational and communication skills, and the ability to work independently in a fast-paced research environment. Join a collaborative, growth-oriented team dedicated to advancing clinical research and making life better through high-quality clinical trials.
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5+ years of clinical research experience
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Experience managing 6–8 clinical studies preferred
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High school diploma or GED required (some college preferred)
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Manage day-to-day operations of assigned clinical trials from startup through closeout.
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Serve as the primary point of contact for sponsors, CROs, monitors, investigators, and participants.
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Ensure protocol compliance, regulatory compliance, and adherence to site SOPs.
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Complete source documentation during participant visits and enter data into EDC within 48 hours.
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Resolve EDC queries within 24 hours.
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Coordinate monitoring visits, investigator meetings, and site initiation visits.
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Perform clinical procedures including:
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Vital signs
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ECGs
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Specimen collection
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Participant interviews
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Maintain regulatory documentation, delegation logs, training logs, drug accountability records, and temperature logs.
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Report adverse events and maintain safety documentation.
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Train and mentor research staff and act as a clinical research subject matter expert.
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Strong organizational and communication skills
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Ability to work independently and collaboratively
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Experience with sponsor communication and clinical trial management
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Familiarity with EDC systems, GCP, regulatory requirements, and clinical documentation
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Ability to work remotely when applicable and be available during business hours
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Ability to lift up to 15 pounds
Tekton Research describes itself as a growth-oriented clinical research organization emphasizing teamwork and the core values of Focus, Discipline, and Accountability.
For more information about the company and its opportunities, visit: Tekton Research
