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Mass General Brigham
Overview
The coordinator assists with clinical research studies by recruiting, evaluating, and consenting patients while collecting and organizing study data. They are also responsible for performing clinical tests like phlebotomy and EKGs and maintaining regulatory documentation.
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Compensation
$20 - $29 / HOUR
Posted
2 days ago
University of Tennessee
The Research Technician 2 supports research on lymphedema and AI in cancer care under the supervision of a Principal Investigator. Responsibilities include managing regulatory paperwork, IRB applications, and preparing study protocols and manuscripts.
$19 / HOUR
3 days ago
Weill Cornell Medical College
The Research Nurse Specialist ensures optimal quality of medical care for patients participating in clinical research studies and assists in the formation of educational materials. They also assess patient eligibility, coordinate informed consent, and monitor adherence to study protocols.
$108,972 - $125,388 / YEAR
5 days ago
$29 / HOUR
7 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
9 days ago
Clinical Research Coordinators manage the day-to-day execution of clinical trials, including coordinating study visits and collecting data. They work directly with patients, investigators, and cross-functional teams to ensure compliance with protocols and regulatory requirements.
$45,000 - $100,000 / YEAR
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.
The Clinical Research Coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests. They also maintain study documentation, prepare data for analysis, and ensure compliance with regulatory protocols.
16 days ago
Nova Medical Services
The Clinical Research Coordinator manages the planning and execution of clinical trials, ensuring strict adherence to ICH, GCP, and regulatory guidelines. Key duties include coordinating patient visits, maintaining regulatory documentation, and managing study data entry and verification.
$23 - $25 / HOUR
17 days ago
University of Massachusetts Medical School
The Research Nurse Coordinator is responsible for carrying out delegated tasks related to complex protocols testing investigational drugs and devices. They act as a liaison between various stakeholders to ensure good clinical practice standards throughout the study lifecycle.
$34 - $53 / HOUR
21 days ago
The coordinator supports clinical research studies on neuromuscular diseases by recruiting and consenting patients and performing clinical tests. They are also responsible for maintaining research data, performing QA/QC checks, and assisting the PI with reports and presentations.
$24 - $39 / HOUR
23 days ago
Washington University in St. Louis
Assists the Principal Investigator in coordinating clinical research studies, ensuring regulatory compliance and IRB support. Manages project infrastructure, including budget oversight, data management via REDCap, and participant coordination.
$23 - $34 / HOUR
29 days ago
Mount Sinai Health System
The Research Program Coordinator develops and participates in study protocols, designs management and statistical plans, and analyzes data. They are responsible for conducting human subjects or laboratory research and preparing final study reports.
$58,661 - $81,675 / YEAR
1 month ago
Beth Israel Lahey Health
Coordinate and administer multiple research studies related to Hypertrophic Cardiomyopathy. Implement study protocols in accordance with regulatory and institutional requirements while collaborating with physicians and research staff.
$19 - $31 / HOUR
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
Nationwide Children's Hospital
Assists with administrative components to ensure regulatory compliance for clinical research projects, including maintaining study binders and files. Prepares and submits IRB documents while ensuring accuracy across regulatory and grant systems.
Assists with administrative components to ensure regulatory compliance for clinical research projects. Responsibilities include maintaining study binders, submitting IRB documents, and collecting investigator credentials.
Sago
The Research Project Interviewer supports study execution by conducting subject interviews, obtaining informed consent, and managing study visits. They also ensure all documentation complies with regulatory requirements and collaborate with the clinical project management team.
$15 / HOUR
University of Pennsylvania
Coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
