Job Details

Title: Clinical Research Coordinator (CRC)Location: Las Vegas, NV & Henderson, NV (Fully Onsite)Contract: 6–12 Month Contract-to-HireStart Date: March 20, 2026Pay Rate: $30-$32/hrOverviewWe are seeking a Clinical Research Coordinator (CRC) to join a growing clinical research program focused on early cancer screening studies. This role will work closely with physicians, pulmonologists, and clinical staff to identify and enroll patients in non-drug, non-device clinical trials conducted within the hospital setting.The coordinator will be responsible for managing study operations, conducting the informed consent process, supporting patient recruitment in the ER, processing lab specimens, and ensuring compliance with IRB, regulatory, and protocol requirements.This is a high-impact role where the coordinator will serve as the primary research professional on the team, helping enable the site to launch and conduct clinical trials.LocationFully onsite across three clinic locations:2 sites in Henderson, NV1 site in Las Vegas, NVKey ResponsibilitiesClinical Trial CoordinationCoordinate site initiation and protocol training for all clinical studies.Conduct the informed consent process with research participants and ensure documentation meets protocol and regulatory requirements.Coordinate and schedule study visits, procedures, and testing in accordance with study protocols.Actively identify, recruit, screen, and enroll participants for early cancer screening trials.Serve as the primary liaison between research participants, physicians, sponsors, and regulatory bodies.Lab & Specimen ManagementCollect and process clinical trial specimens including centrifuging, aliquoting, and preparing samples for shipment.Ship biological specimens in compliance with federal biologics shipping regulations.Support protocol-required procedures such as blood draws, ECGs, and clinical assessments (when credentialed).Data & Regulatory ComplianceCollect, document, and report study data accurately in accordance with protocol requirements, regulatory guidelines, and institutional policies.Prepare and maintain regulatory documentation, including:IRB submissionsInformed consent documentationFDA Form 1572Conflict of Interest formsStudy binders and participant chartsCreate and maintain source documentation templates to ensure accurate data collection.Identify and report adverse events, protocol deviations, and safety issues in compliance with regulatory requirements.Study Management & Quality AssuranceEnsure clinical trials comply with FDA, Good Clinical Practice (GCP), and human research protection regulations.Support site feasibility assessments for potential new research studies.Coordinate sponsor monitoring visits, audits, and data queries.Implement quality improvement processes to ensure protocol adherence and regulatory compliance.CollaborationWork closely with Principal Investigators, physicians, pulmonologists, and hospital staff to ensure protocol adherence.Attend investigator meetings and study-related training sessions as required.Coordinate with research administration and clinical teams to support study operations.Required Qualifications2+ years of Clinical Research Coordinator (CRC) experienceCRC Certification requiredExperience with clinical trial regulatory documentation and IRB processesLab processing experience required (centrifuging, aliquoting, specimen handling)Experience conducting informed consent with study participantsStrong knowledge of GCP, FDA, and clinical research regulationsPreferred QualificationsClinical background in Neurology, Cardiology, or OncologyPhlebotomy certificationExperience working in hospital or emergency department settings