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Iterative Health
Overview
The Clinical Research Coordinator I supports and coordinates daily clinical trial activities, including administratively and clinically managing industry-sponsored trials, problem-solving, and ensuring protocol adherence. Key duties involve leading patient recruitment, scheduling visits, conducting procedures like blood draws and injections, and dispensing study medication.
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Compensation
Salary not listed
Posted
2 days ago
Avera Health
Coordinates and implements research study protocols, including participant recruitment, screening, and data collection. Manages laboratory specimens and ensures compliance with FDA regulations and Good Clinical Practices.
$22 - $37 / HOUR
4 days ago
Clinilabs
The Polysomnographic Technologist prepares and collects data for research and clinical duties, ensuring the accuracy of recording procedures. Responsibilities also include direct contact with subjects for assessments and maintaining laboratory equipment.
$47 - $55 / HOUR
6 days ago
Evolution Research Group
The EMT/Paramedic assists in clinical trials by dispensing investigational drugs and collecting biological samples. They are responsible for performing ECGs, venipuncture, and ensuring all procedures follow Good Clinical Practices (GCP).
9 days ago
The Unit Clinician assists with clinical trial execution by performing procedures such as venipuncture, ECGs, and biological sample processing. They are responsible for dispensing investigational products and maintaining accurate documentation in subject charts according to protocol.
$39 - $45 / HOUR
The LPN or RN will assist in the conduct of clinical trials by dispensing investigational drugs and collecting biological samples. They are responsible for performing clinical procedures, maintaining accurate subject charts, and ensuring compliance with Good Clinical Practices.
Glaukos
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
$73,600 - $85,000 / YEAR
The CRC II manages industry-sponsored clinical trials, overseeing patient recruitment, study visits, and the collection of clinical data. They are responsible for maintaining high-quality documentation and coordinating communication between sponsors, CROs, and the Principal Investigator.
14 days ago
University of California, Irvine
Coordinate and manage Phase I-IV cancer-related clinical trials, ensuring adherence to GCP, SOPs, and university policies. Act as a liaison between sponsors, regulatory agencies, and the research team while managing patient recruitment and data collection.
15 days ago
Care Access
The Clinical Research Coordinator I, RN conducts delegated clinical tasks and monitors research participants to ensure compliance with protocols and regulations. They are responsible for patient coordination, documentation, and recruitment activities.
20 days ago
San Francisco AIDS Foundation
Perform high-volume phlebotomy and manage the processing and quality assurance of laboratory specimens. Additionally, serve as an HIV testing counselor providing education and prevention services to at-risk communities.
$34 - $37 / HOUR
23 days ago
Perform high-volume phlebotomy and manage the processing and transport of laboratory specimens. Conduct quality assurance on tests and serve as an HIV testing counselor to provide patient education.
Baptist Health South Florida
The Nurse Research Coordinator supports the Clinical Research staff by coordinating and administering clinical study protocols in cooperation with the Principal Investigator. This role includes ensuring compliance with regulatory requirements and maximizing subject participation in cardiovascular research protocols.
26 days ago
LUX Infusion
The Clinical Pharmacist is responsible for verifying prescriptions, conducting clinical reviews of patient therapies, and ensuring safe medication dispensing. They also collaborate with internal teams to support patient onboarding and maintain compliance with federal and state pharmacy standards.
$130,000 - $140,000 / YEAR
27 days ago
Highmark Health
The role involves planning and managing clinical trials while ensuring compliance with regulatory bodies and human subject research standards. Key duties include identifying eligible patients, providing education to staff and participants, and maintaining clinical data and regulatory binders.
29 days ago
Hoag
The Clinical Research Coordinator II manages all facets of clinical research trials, including planning, implementation, and closure, ensuring smooth and accurate processes in cooperation with physicians and sponsors. Responsibilities include protocol review, obtaining informed consent, managing study documentation, data collection, sample processing according to IATA standards, and adverse event reporting.
$37 - $57 / HOUR
1 month ago
NYU Langone Health
The Research Coordinator manages the coordination of research studies, including participant recruitment, enrollment, and data collection. They ensure protocol execution follows Good Clinical Practices and HIPAA regulations while interfacing with patients and principal investigators.
$66,300 - $68,250 / YEAR
The Assistant Clinical Research Coordinator supports cancer-related clinical trials by managing data, coordinating protocol requirements, and assisting the Principal Investigator with patient recruitment and screening. They also serve as a liaison between sponsors, regulatory agencies, and the research team to ensure compliance with institutional and federal policies.
The Clinical Research Coordinator will manage clinical trial data and support research operations in compliance with Good Clinical Practices and internal policies. Responsibilities include patient recruitment, screening, consenting, and preparing regulatory submissions for the IRB and other committees.
The Clinical Research Coordinator manages the initiation and completion of clinical trials while ensuring compliance with regulatory standards and patient safety. They interface with clinical staff and patients to provide education, obtain informed consent, and maintain accurate clinical data.
