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Mass General Brigham
Overview
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.
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Compensation
$20 - $29 / HOUR
Posted
2 days ago
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.
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
9 days ago
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.
13 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.
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.
Mount Sinai Health System
The Clinical Research Assistant assists in daily research activities, including the collection and organization of study information. They also provide clerical support to coordinators and assist in the preparation of grant applications and regulatory documents.
$17 - $25 / HOUR
The Clinical Research Coordinator assists in conducting clinical research studies under the supervision of the Principal Investigator. Responsibilities include obtaining informed consent, managing study data, and preparing grant and regulatory submissions.
$17 - $41 / HOUR
MAPMG
The Clinical Research Nurse coordinates the clinical trial study process, including patient recruitment, informed consent, and protocol-required procedures. They also ensure regulatory compliance, maintain accurate study documentation, and monitor patient outcomes throughout the study lifecycle.
$79,370 - $99,213 / YEAR
University of Rochester
The specialist is responsible for the coordination and oversight of regulatory requirements for clinical research protocols. They manage documentation, maintain logs in tracking systems, and act as a liaison between study teams, sponsors, and regulatory committees.
$25 - $35 / HOUR
University of Virginia
This role involves coordinating and implementing clinical trial research studies, working closely with Principal Investigators on all assigned projects, which includes managing recruitment, obtaining informed consent, and overseeing ongoing study conduct activities. Responsibilities also cover preparing and submitting all necessary regulatory documentation to the IRB, managing study billing reconciliation, and ensuring effective communication with study Sponsors.
2 months ago
