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Arizona Liver HealthNew
Overview
Coordinate clinical research trials by recruiting participants, performing clinical procedures like phlebotomy and vitals, and managing study data. Ensure strict adherence to regulatory guidelines, maintain study documentation, and collaborate with sponsors and internal staff.
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Compensation
$28 - $36 / HOUR
Posted
New
Fortrea
The Research Nurse will deliver high-quality care to trial participants, monitor their well-being, and respond to emergencies while administering investigational compounds and performing study procedures like ECGs and venipuncture. Responsibilities also include collecting and processing biological samples and ensuring strict adherence and accurate record-keeping for clinical protocols.
Salary not listed
2 days ago
Avera Health
Coordinates and implements research study protocols, including participant recruitment, data collection, and laboratory specimen processing. Collaborates with investigators and healthcare providers to ensure safe, compliant research procedures for maternal and child health studies.
$21 - $37 / HOUR
4 days ago
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 C Medical Technologies
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
$75,000 - $95,000 / YEAR
6 days ago
Headlands Research
The Laboratory Technician performs specimen collection, processing, documentation, and shipment for clinical trials in compliance with GCP and study protocols, while also assisting with vital signs, ECGs, and maintaining laboratory equipment and cleanliness. Responsibilities also include accurate data recording, resolving data queries, monitoring lab inventory, and supporting study preparation activities.
$22 - $26 / HOUR
Care Access
This event-based role involves supporting participant care and clinical research event operations, including performing phlebotomy, handling biospecimens, and accurately documenting all procedures according to regulatory standards. Responsibilities also include setting up and managing event stations, ensuring smooth operations, and maintaining compliance and participant safety.
$44 / HOUR
7 days ago
Nevada System of Higher Education
The Research Coordinator will recruit and screen clinical trial participants, manage regulatory documentation, and provide clinical care services including patient monitoring and sample processing. They will also assist with study budget proposals, data entry, and ensure adherence to institutional and federal protocols.
$25 - $37 / HOUR
8 days ago
Evolution Research Group
The Psychometric Rater is responsible for administering and scoring clinical tests and managing data collection for clinical trials. They collaborate with researchers to ensure strict adherence to study protocols, ethical guidelines, and FDA regulations.
$30 / HOUR
9 days ago
The Psychometric Rater is responsible for administering and scoring tests for clinical trial participants while ensuring strict adherence to study protocols and ethical guidelines. They collaborate with researchers to collect accurate data and manage participant documentation under the direction of the Principal Investigator.
$34 / HOUR
The Clinical Research Coordinator manages the implementation of clinical trials, including subject screening, enrollment, and the administration of study procedures. They ensure all activities comply with FDA regulations, GCP guidelines, and company SOPs while maintaining accurate study documentation.
The Clinical Research Coordinator manages the implementation of clinical trials, ensuring adherence to protocols and regulatory requirements. They are responsible for screening and enrolling subjects, maintaining accurate study records, and reporting adverse events under the direction of the Principal Investigator.
American Clinical Research Services Opco LLC
The Clinical Research Coordinator manages clinical trials by overseeing subject recruitment, dosing, and data collection while ensuring regulatory compliance. They collaborate with investigators to maintain study documentation and monitor participant progress throughout the trial.
$50,000 - $67,000 / YEAR
14 days ago
This event-based role involves supporting participant care and clinical research event operations, including performing phlebotomy, handling specimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing event stations, guiding participants through the flow, and maintaining a safe, compliant workspace.
University of New Mexico
The Research Coordinator will support clinical investigators in conducting dermatology clinical trials, including recruiting subjects and coordinating research activities. Responsibilities also include data collection, safety reporting, and maintaining compliance with regulatory guidelines.
$20 - $27 / HOUR
23 days ago
Inotiv
Responsible for the daily care, husbandry, and well-being of laboratory animals in compliance with SOPs and federal regulations. Duties include facility upkeep, monitoring animal health, and assisting with in-life study conduct and data collection.
$18 - $20 / HOUR
24 days ago
Ann & Robert H. Lurie Children's Hospital of Chicago
The coordinator supports the GROWTH study by managing regulatory documents, recruiting eligible subjects, and collecting and processing specimens. They are also responsible for data entry into electronic platforms and coordinating study visits and reimbursements.
$46,280 - $75,670 / YEAR
University of Miami
The coordinator manages simple clinical research protocols, including participant screening, data collection, and maintenance of regulatory binders. They are responsible for recruiting patients, obtaining informed consent, and ensuring adherence to international and local regulatory standards.
25 days ago
Coordinates the planning, implementation, and monitoring of clinical research studies from initiation to close-out. Manages participant recruitment, data collection, and regulatory documentation while ensuring adherence to safety protocols.
The coordinator supports clinical trials for rare genetic disorders by managing regulatory documents and recruiting eligible study subjects. They are also responsible for collecting specimens, entering data into electronic platforms, and coordinating study visits.
$22 - $36 / HOUR
27 days ago
