Find Jobs in the USA

Pantheon Clinical Research is seeking a Clinical Research Coordinator to manage active industry-sponsored clinical trials. The role oversees study operations, participant visits, sponsor interactions, data collection, and regulatory compliance while supporting high-quality patient care. Responsibilities Coordinate day-to-day operations of assigned clinical trials Screen, consent, enroll, and schedule study participan

Kinetic Systems is an applied AI research lab developing practical AI solutions for healthcare challenges. The Clinical Research Coordinator role helps the team understand clinical trial operations by creating and reviewing realistic work scenarios and explaining day-to-day workflows. Responsibilities Write and refine realistic work scenarios Review scenarios written by other coordinators for accuracy and realism Wal

Goldbelt Apex LLC is a data-focused healthcare technology company supporting healthcare organizations with data communication and exchange systems. The Clinical Research Coordinator will independently coordinate complex clinical and biomedical research activities for the Defense Health Agency Clinical Investigation Program at Naval Medical Center Portsmouth, including protocol execution, regulatory compliance, resear

Responsibilities Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines Provide medical care to patients, always ensuring patient safety comes first Schedule subject visits within protocol windows, ensuring scheduling capacity is maximized Perform all defined study activities (i.e., informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnan

Phoenix Children's seeks a Clinical Research Coordinator 2 to coordinate research projects from pre-study implementation through study closure. The role independently manages study data and specimens, regulatory documentation, participant recruitment and scheduling, and protocol-related research activities. Responsibilities Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FD

Responsibilities Screens potential participants for protocol eligibility Presents trial concepts and details to participants, participates in the informed consent process, and enrolls participants into clinical trials Coordinates participant care in compliance with protocol requirements May disburse investigational product and maintain accountability records Oversees preparation of orders by providers to ensure proto

The University of Wisconsin–Madison is hiring a Clinical Research Coordinator for its Department of Orthopedics & Rehabilitation, Division of Sports Medicine. The role coordinates investigator-initiated and industry-sponsored research, including participant screening and data collection, study workflow and regulatory support, and research reporting and dissemination. Responsibilities Screen patients for eligibility a

Responsibilities Performs all aspects of research related job duties in accordance with site-specific standard operating procedures in coordination with the Allergy Partners physician designated as the study Principal Investigator Maintain required certifications as assigned Follow all federal, state, and local guidelines regarding clinical trials Provides assistance to Practice Manager, Clinical Coordinator, and Pro

Health Marketing is hiring a Clinical Research Coordinator to support clinical research activities and maintain effective relationships with investigators, healthcare professionals, and team members. The role ensures research studies comply with applicable regulatory and ethical guidelines and supports study processes, documentation, and participant management. Responsibilities Collaborate with investigators and heal

Adult Pediatric Urology & Urogynecology is hiring a Clinical Research Coordinator to coordinate clinical research studies, including participant recruitment, screening, and enrollment. The role manages study visits, consent, data and regulatory documentation, compliance, collaboration, monitoring and audit preparation, reporting, and study closeout. Responsibilities This position is responsible for coordinating clini

United Consulting Hub seeks a Clinical Research Coordinator to support the coordination and execution of clinical research studies and trial activities. The role focuses on study documentation, site and patient coordination, clinical data management, study tracking, and compliance with approved protocols, regulations, and quality standards. Responsibilities Support the day-to-day coordination and execution of assigne

Responsibilities Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality Conduct clinical research as outlined in the study protocol. Maintain knowledge of clinical research issues. Follow GCP guidelines. Implement confidentiality and

DelRicht Research is a clinical research company conducting clinical trials to support the approval of new medications and medical devices. The Clinical Research Coordinator supports patient experience and accurate, efficient study execution across the company’s Vienna and Rockville clinics, including recruitment, visit coordination, data entry, and communication with research stakeholders. Responsibilities Patients

National Institute of Clinical Research (NICR) is hiring a Clinical Research Coordinator to manage clinical studies from initiation through closeout. The role oversees trial operations, protocol adherence, regulatory compliance, study visits, documentation, and collaboration with investigators, sponsors, and clinical staff. Responsibilities Manage clinical studies from placement through study closeout Oversee daily t

Retina Specialty Institute and Southern Eye Group are seeking a Clinical Research Coordinator to support ophthalmic clinical trials. The role coordinates daily study activities and helps ensure compliance with protocols, regulatory requirements, and Good Clinical Practice while supporting patients and the clinical trials team. Responsibilities Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and

Responsibilities Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines Provide medical care to patients, always ensuring patient safety comes first Perform all defined study activities (i.e, informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.) Phlebotomy and sample processing/shipping Record all

Hackensack Meridian Health is hiring a Clinical Research Coordinator to coordinate and oversee assigned clinical trials under the general supervision of the principal investigator. The role supports compliant study conduct, research operations, participant enrollment and follow-up, regulatory documentation, and coordination with investigators, sponsors, and clinical teams. Responsibilities Acts as liaison between pri

Intermountain Health is hiring a Clinical Research Coordinator to coordinate and manage clinical studies across its system. The role supports study execution, regulatory compliance, participant care, research team education, and laboratory operations. Responsibilities Research Support: Support various research studies across the Intermountain system, working on complex or large projects with limited supervision, demo

Indiana University is an institution whose Division of Cardiovascular Medicine conducts cardiovascular research, education, patient care, and clinical trials. The Clinical Research Coordinator manages clinical research studies by supporting protocol review and design, participant recruitment and assessment, regulatory compliance, budgeting, adverse event reporting, and study documentation. Responsibilities Initiates

Responsibilities Coordinate all aspects of assigned clinical trials from site initiation to study close-out Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs Manage subject recruitment, informed consent, and retention strategies Ensure timely data entry and resolutio