Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
Phoenix
Arizona
1497 live openings
Philadelphia
Pennsylvania
1416 live openings
Atlanta
Georgia
1379 live openings
Indianapolis
Indiana
1374 live openings
Legal
VitalHires helps educators discover verified school and district opportunities. Confirm compensation, credentials, and deadlines on the official hiring site before applying.
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.
Quick view →
Compensation
$20 - $29 / HOUR
Posted
3 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
4 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
8 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
10 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.
ICON plc
The Clinical Research Nurse is responsible for coordinating and conducting clinical trial procedures according to protocol requirements. This includes performing technical clinical tasks, documenting patient data, and collaborating with interdisciplinary teams to ensure trial compliance.
11 days ago
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.
17 days ago
The role blends direct patient care, including advanced assessment and emergency response, with clinical research operational tasks. Responsibilities include executing study protocols, maintaining audit-ready documentation, and ensuring participant safety.
18 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
University of Chicago
The Research Coordinator manages day-to-day operations of funded projects focusing on HIV elimination, COVID testing, and substance use. Key duties include recruiting and consenting participants, delivering interventions, and supporting data management and grant writing.
$24 - $29 / HOUR
22 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
Mayo Clinic
Assists in coordinating study details, including patient scheduling, data collection, and maintaining study databases. Performs administrative duties and may conduct technical tasks related to clinical and experimental research under supervision.
$19 - $26 / HOUR
Southcoast Health System, Inc.
Coordinate all activities related to clinical trials, including patient screening, follow-up, and correspondence with the Institutional Review Board and sponsors. Manage trial implementation, budget negotiations, and ensure strict adherence to federal and institutional guidelines for human subject research.
$57,554 - $96,762 / YEAR
24 days ago
Support the design, execution, and management of clinical trials by ensuring accurate data collection and analysis. Maintain organized research documentation and collaborate with cross-functional teams to meet study timelines.
Fortrea
Coordinate and execute the screening and eligibility determination of volunteers for early phase clinical trials. This includes conducting clinical tasks like vitals and ECGs, obtaining informed consent, and maintaining participant data in databases.
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
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
1 month 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
