Clinical Research Coordinator

Job Description

Denver, Colorado | On-Site

A rapidly growing clinical research site network is seeking an experienced Clinical Research Coordinator (CRC) to join its Denver, Colorado team.

This is an excellent opportunity for a hands-on CRC who enjoys a fast-paced, patient-facing research environment and wants to work across a diverse portfolio of clinical trials.

The ideal candidate will have strong experience coordinating clinical trials from start-up through close-out, with a genuine focus on patient care, recruitment, data quality and study execution

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Key Responsibilities

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• Coordinate clinical research studies in accordance with protocols, GCP and applicable regulations.
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• Conduct patient-facing study visits, including screening, enrollment, follow-up and end-of-study visits .
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• Support patient recruitment, prescreening, scheduling and retention activities.
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• Perform and document clinical procedures including:
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• Vital signs
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• 12-lead ECGs
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• Phlebotomy / blood draws
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• Specimen processing and shipment
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• Medication administration, where applicable
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• Collection of medical history and source documentation
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• Maintain accurate and complete source documentation and study records.
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• Complete EDC entries and respond to data queries within required timelines.
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• Coordinate with Principal Investigators, Sub-Investigators, sponsors, CROs and other study stakeholders.
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• Ensure study activities remain compliant with GCP, FDA regulations, protocols and SOPs .
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• Support monitoring visits, audits and inspection readiness.
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• Manage study supplies, investigational product accountability and laboratory requirements where applicable.
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• Identify and escalate protocol deviations, safety concerns and operational issues.
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• Maintain strong communication with study participants throughout the clinical trial journey.#
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Ideal Background

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• Previous experience as a Clinical Research Coordinator within a clinical research site.
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• Experience working directly with study participants in a busy research environment.
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• Strong knowledge of GCP and clinical trial processes .
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• Hands-on experience with vital signs, ECGs and phlebotomy strongly preferred.
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• Experience supporting patient recruitment and retention.
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• Ability to manage multiple protocols and priorities simultaneously.
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• Strong attention to detail and accurate documentation skills.
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• Excellent communication and interpersonal skills.
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• Comfortable working independently while contributing to a collaborative site team.
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• Experience across Phase I–IV clinical trials is highly desirable.
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• Exposure to areas such as metabolic, cardiology, CNS, respiratory, infectious disease or vaccine research would be advantageous.
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What’s on Offer

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• Opportunity to join a high-growth clinical research organization .
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• Exposure to a diverse and expanding clinical trial portfolio.
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• Hands-on, patient-facing research environment.
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• Strong opportunities for professional development and progression.
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• Collaborative and supportive clinical research team.
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• Competitive salary and benefits package.
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• Opportunity to build a long-term career within a growing research network.
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