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Mass General Brigham
Overview
The Clinical Research Coordinator manages day-to-day operations of clinical research studies, including participant recruitment, data collection, and study visit coordination. They ensure protocol compliance and handle regulatory documentation and IRB submissions.
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Compensation
$29 / HOUR
Posted
2 days ago
The coordinator will assist with clinical research studies by recruiting, evaluating, and consenting patients, collecting and organizing patient data, and scheduling study visits. Key duties also involve performing clinical tests like phlebotomy and EKGs, and maintaining study documentation and data integrity.
$20 - $29 / HOUR
This role supports research studies in Sleep and Circadian Disorders by instructing subjects, obtaining informed consent, collecting, organizing, and analyzing study data, and preparing regulatory documentation. Responsibilities also include creating REDCap surveys and databases, training personnel, and troubleshooting specialized data collection devices during various shifts.
Visionary Ophthalmology
The coordinator manages day-to-day activities for ophthalmology clinical trials, including subject visits and regulatory compliance. They are responsible for data entry, maintaining study binders, and communicating with sponsors and CROs.
$25 - $30 / HOUR
9 days ago
Headlands Research
The Clinical Research Coordinator will manage and execute Phase II-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaborating with investigators and lab teams to maintain study integrity.
Salary not listed
The Clinical Research Coordinator manages and executes Phase I-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaboration with investigators and sponsors.
Coordinate all aspects of assigned clinical trials from site initiation to study close-out, ensuring compliance with study protocols and regulations. Manage subject recruitment, conduct visits, and maintain accurate documentation throughout the trial process.
Ora
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks and collaborate with project managers and investigators to execute research directives.
14 days ago
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks, manage study documentation, and collaborate with investigators and project managers.
New York State Psychiatry Institute
The Research Coordinator will assist with study implementation, regulatory management, and participant coordination. They will oversee daily trial operations and ensure protocol adherence.
$46,021 - $54,975 / YEAR
24 days ago
Gentiva Hospice
Provide high-quality nursing care and implement individualized plans for hospice patients across multiple regional locations. Support interdisciplinary teams and educate families on care instructions and safety protocols.
City of Hope
The Clinical Research Nurse coordinates oncology clinical trials, managing everything from patient recruitment and informed consent to data collection and biospecimen handling. They ensure strict adherence to federal regulations, study protocols, and institutional SOPs to protect human subjects.
28 days ago
Velocity Clinical Research, Inc.
The Clinical Research Assistant supports the Clinical Operations Team by collecting, documenting, and maintaining clinical data. Key duties include performing phlebotomy, processing laboratory specimens, and managing administrative tasks such as data entry and patient scheduling.
1 month ago
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks and collaborate with internal and external teams to execute research directives.
University of Oklahoma
Coordinate multiple cancer outcomes research protocols, including participant enrollment and data management using REDCap and OnCore. Collaborate with principal investigators and the IRB to develop protocols and contribute to manuscript development.
University of Chicago
The Clinical Research Coordinator I facilitates daily clinical research activities, including participant screening, enrollment, and data collection. They ensure study compliance with federal and institutional regulations while maintaining accurate documentation and coordinating patient schedules.
$50,000 - $65,000 / YEAR
HonorHealth
The coordinator facilitates regulatory affairs for clinical research, ensuring compliance with FDA, ICH, and IRB standards. They manage study protocols from startup through closure, including document preparation and regulatory correspondence.
The New Jewish Home
The Registered Dietitian will conduct comprehensive nutrition assessments and develop individualized care plans for residents in long-term and sub-acute care. They will also perform meal rounds and collaborate with the interdisciplinary healthcare team to ensure quality resident outcomes.
