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UVA HealthNew
Overview
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary research teams to support the advancement of cancer research.
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Compensation
$28 - $81,500 / HOUR
Posted
New
IQVIA
The intern supports the preparation, documentation, and management of investigational products for clinical trials under pharmacist supervision. Key duties include managing drug accountability logs, dispensing medications per protocol, and ensuring regulatory compliance with FDA and IRB standards.
$33,000 - $82,600 / YEAR
2 days ago
Ann & Robert H. Lurie Children's Hospital of Chicago
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing documents, managing study conduct across departments, and overseeing all aspects of clinical research visits. Responsibilities also include managing participant engagement, collecting specimens, recording data, assisting with financial aspects, and participating in investigator meetings.
$49,920 - $81,619 / YEAR
6 days ago
University of Virginia
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary teams to support the advancement of innovative cancer research.
9 days ago
Mayo Clinic
The RN Study Coordinator is responsible for coordinating and delivering nursing care, including direct patient care and education in clinical and research settings. They manage all phases of the research process and ensure compliance with regulatory laws and institutional guidelines.
$30 - $52 / HOUR
1 month ago
UCSF
The Clinical Research Coordinator manages and coordinates research protocols for pediatric diabetes studies, including participant recruitment and data collection. They oversee regulatory compliance, maintain study documentation, and facilitate communication between clinical staff, families, and investigators.
Salary not listed
Coordinates behavioral research projects by managing study start-up, regulatory documentation, and participant recruitment. Conducts research visits, administers behavioral interventions, and performs data entry and quality assurance under PI supervision.
West Virginia University
The Clinical Research Specialist will coordinate and implement operational tasks for neuromodulation brain therapeutics research projects. Responsibilities include ensuring protocol compliance, managing patient care, facilitating informed consent, and maintaining accurate research documentation.
University of Rochester
The Human Subject Research Specialist II coordinates clinical trial activities, including participant enrollment, protocol implementation, and data management within the infectious disease division. They ensure compliance with regulatory standards, maintain research records, and assist with quality assurance audits.
$25 - $35 / HOUR
The Clinical Research Coordinator will independently manage complex Alzheimer's disease research protocols, including participant recruitment, data monitoring, and regulatory compliance. The role also involves direct administration of neuropsychometric testing and cognitive assessments as a core responsibility.
$28 - $42 / HOUR
University of Miami
The Clinical Research Coordinator 2 assists in the planning, implementation, and monitoring of clinical research studies, specifically focusing on genetic studies of Alzheimer's disease in African Ancestry communities. Responsibilities include participant recruitment, data collection, biological sample processing, and ensuring adherence to regulatory and protocol guidelines.
2 months ago
St. Jude Children's Research Hospital
Postdoctoral fellows will be trained to lead independent research programs in the discovery of therapeutics for infectious diseases. The program includes collaborations across various departments to develop therapies and understand the biology of infections.
Washington University in St. Louis
The postdoctoral researcher will lead a project focused on tear gland development and management of dry eye disease. Responsibilities include assisting with grant preparation, designing research experiments, and reporting research findings.
The Clinical Research Coordinator will manage and execute research protocols, oversee data integrity, and coordinate participant visits for clinical studies. They will act as a liaison between departments and ensure compliance with regulatory agencies and institutional policies.
This role coordinates all aspects of clinical research projects, overseeing activities from study start-up through close-out while ensuring strict adherence to protocols and regulatory requirements. Key functions include managing regulatory documentation, participant engagement, data lifecycle management, and assisting with financial and dissemination activities.
$59,280 - $96,928 / YEAR
Lurie Children's Hospital
This role coordinates all aspects of clinical research projects, overseeing activities from study start-up through close-out while ensuring strict adherence to protocols and regulatory requirements. Key functions include managing regulatory documentation, participant engagement, data lifecycle management, and leading the dissemination of research findings.
3 months ago
