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Responsibilities Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials Ensuring protocol compliance, data integrity, and patient safety throughout the trial process Collaborating with investigators and site staff to facilitate smooth study conduct Performing data review and resolution of queries to maintain high-quality clinical data Contributing to the preparation and review

RegenTX, LLC is hiring a Clinical Research Associate to oversee operational aspects of clinical trials at investigational sites. The role monitors site performance, supports regulatory compliance and data integrity, and coordinates study activities across multiple trials. Responsibilities Evaluate clinical trial resourcing requirements for qualification (SQVs), training (SIVs), monitoring (IMVs) and support of sites

Alira Health is a global team focused on innovation and collaboration. They are seeking a Clinical Research Associate who will conduct site monitoring for clinical trials, ensuring protocol compliance and assisting with various site-related issues. Responsibilities Performs qualification, initiation, interim, and close-out visits and ensures proper documentation of site visits Prepares consistently accurate and timel

Alira Health is a global team dedicated to innovation and collaboration. The Clinical Research Associate will conduct site monitoring responsibilities for clinical trials, ensuring protocol compliance and assisting with site-related issues. Responsibilities Performs qualification, initiation, interim, and close-out visits and ensures proper documentation of site visits Prepares consistently accurate and timely monito

Alira Health is seeking a Clinical Research Associate to independently conduct and oversee clinical trial site monitoring activities while ensuring protocol compliance, quality, and regulatory adherence. The role manages site visits, monitoring documentation, data verification, investigator relationships, issue resolution, and CRA team support. Responsibilities Provides guidance, oversight, and feedback to the CRA te

Yale University is hiring a Clinical Research Associate to implement clinical research operations in the Testani laboratory. The role supports heart failure studies through participant recruitment and consent, accurate data and regulatory management, study procedures, and biospecimen processing. Responsibilities Implementation of the clinical research operation of the Testani laboratory; will be responsible for worki

Responsibilities Assembles data and performs quality control checks to ensure the accuracy and reliability of research findings, contributing to the validity and credibility of research outcomes and enabling evidence-based decision-making Contributes to early-stage activities for research projects, including subject recruitment, literature gathering, and Institutional Review Board (IRB) document submission, facilitat

Responsibilities Conduct site qualification, initiation, monitoring, and closeout visits Provide training and support to investigators, study coordinators, and site staff Monitor protocol compliance, data quality, and Good Clinical Practice (GCP) requirements Review source documents and verify clinical study data for accuracy and completeness Ensure only eligible participants are enrolled in studies Manage and mainta

Ardence Consulting is recruiting for an unnamed medical device client seeking a Clinical Research Associate to support ongoing clinical trials. The role focuses on clinical trial monitoring, query closure, risk-based studies, TMF creation, and site management. Responsibilities Ensure site reporting/compliance Conduct study startup, monitoring, closeout visits Support the clinical team with investigator meetings Assis

ICON Strategic Solutions is hiring a sponsor-dedicated Clinical Research Associate to support a client’s cardiovascular and obesity trials. The role monitors clinical trials, ensuring protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff. Responsibilities Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials Ensuring pro

Allergan Aesthetics, an AbbVie Company, is hiring a Clinical Research Associate to support clinical research and advance AbbVie’s pipeline. The role partners with investigators and site staff to oversee trial conduct, strengthen data integrity and compliance, support patient recruitment, and manage site performance and safety. Responsibilities Considered as the primary point of contact for the investigative site. Hig

SoTalent is recruiting for an employer that is not identified by name. The Clinical Research Associate will monitor solid tumour oncology trials, oversee site compliance and data quality, support participant recruitment, and coordinate with sites and study teams throughout the study lifecycle. Responsibilities Coordinate and conduct site qualification, activation, routine monitoring, and study closure visits in accor

Globus Medical develops innovations to improve the quality of life of patients with musculoskeletal disorders and improve surgical techniques and outcomes. The Clinical Research Associate monitors and supports clinical study sites, ensuring participant safety, clinical data integrity, protocol compliance, and regulatory adherence. The role serves as a liaison between the sponsor and investigational sites and collabor

The employer is a global medical device company specializing in minimally invasive targeted tumor treatment technologies and interventional oncology clinical studies. The Clinical Research Associate will coordinate study activities, support and monitor clinical research sites, maintain documentation and data quality, and ensure compliance with protocols, GCP, regulations, and patient safety requirements. Responsibili

Orca Bio is a commercial-stage biotechnology company developing next-generation cell therapies to improve outcomes for patients with blood cancer. The Clinical Research Associate will monitor clinical studies at investigative sites or remotely, ensuring trials are conducted, documented, and reported according to protocols, SOPs, ICH-GCP, and applicable regulations. Responsibilities May serve as the primary monitor an

Responsibilities Identify, assess, and initiate investigational sites Conduct feasibility, pre-study, initiation, monitoring, and close-out visits Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements Perform source data verification and ensure data accuracy and completeness Monitor patient recruitment and support sites in meeting targets Ensure proper reporting of adverse events and protocol d

Allucent is a biopharmaceutical clinical research organization that helps small and medium-sized biopharmaceutical companies navigate clinical trials. The Clinical Research Associate will independently manage monitoring activities, maintain site relationships, ensure protocol and regulatory compliance, resolve site issues, and mentor junior CRAs while traveling throughout the United States. Responsibilities Independe

ICON Strategic Solutions is a sponsor-dedicated clinical research organization that provides global expertise and supports the development of treatments benefiting patients worldwide. The Clinical Research Associate will conduct and monitor clinical trials in multiple therapeutic areas, including oncology, while ensuring protocol compliance, data integrity, and patient safety. The role also involves collaborating wit

NYU Langone Health is an academic medical and research institution committed to medical education, scientific research, patient care, equity, and inclusion. The Clinical Research Associate will support clinical trials and cohort studies through participant recruitment, clinical data collection, study coordination, specimen processing, database maintenance, regulatory compliance, and research reporting, primarily in d

Mass General Brigham is a not-for-profit healthcare organization supporting patient care, research, teaching, and community service. The Clinical Research Associate ensures that clinical trial regulatory requirements are met by managing regulatory documentation, submitting materials to institutional and federal entities, and coordinating with clinical teams, IRBs, sponsors, and regulatory agencies. Responsibilities M