Clinical Research Coordinator

Denver, Colorado | On-SiteDo not pass up this chance, apply quickly if your experience and skills match what is in the following description.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 executionKey ResponsibilitiesCoordinate clinical research studies in accordance with protocols, GCP and applicable regulations.Conduct patient-facing study visits, including screening, enrollment, follow-up and end-of-study visitsSupport patient recruitment, prescreening, scheduling and retention activities.Perform and document clinical procedures including:Vital signs12-lead ECGsPhlebotomy / blood drawsSpecimen processing and shipmentMedication administration, where applicableCollection of medical history and source documentationMaintain accurate and complete source documentation and study records.Complete EDC entries and respond to data queries within required timelines.Coordinate with Principal Investigators, Sub-Investigators, sponsors, CROs and other study stakeholders.Ensure study activities remain compliant with GCP, FDA regulations, protocols and SOPsSupport monitoring visits, audits and inspection readiness.Manage study supplies, investigational product accountability and laboratory requirements where applicable.Identify and escalate protocol deviations, safety concerns and operational issues.Maintain strong communication with study participants throughout the clinical trial journey.#Ideal BackgroundPrevious experience as a Clinical Research Coordinator within a clinical research site.Experience working directly with study participants in a busy research environment.Strong knowledge of GCP and clinical trial processesHands-on experience with vital signs, ECGs and phlebotomy strongly preferred.Experience supporting patient recruitment and retention.Ability to manage multiple protocols and priorities simultaneously.Strong attention to detail and accurate documentation skills.Excellent communication and interpersonal skills.Comfortable working independently while contributing to a collaborative site team.Experience across Phase I–IV clinical trials is highly desirable.Exposure to areas such as metabolic, cardiology, CNS, respiratory, infectious disease or vaccine research would be advantageous.What's on OfferOpportunity to join a high-growth clinical research organizationExposure to a diverse and expanding clinical trial portfolio.Hands-on, patient-facing research environment.Strong opportunities for professional development and progression.Collaborative and supportive clinical research team.Competitive salary and benefits package. xhyhwjd Opportunity to build a long-term career within a growing research network.