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Medical University of South CarolinaNew
Overview
The incumbent will coordinate the recruitment, screening, and enrollment of research participants while collecting psychological and biological data. They are also responsible for maintaining regulatory documentation and providing administrative support for grant proposals and publications.
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Compensation
$37,200 - $59,500 / YEAR
Posted
New
Arizona Liver HealthNew
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.
$28 - $36 / HOUR
American Addiction Centers
Coordinates clinical and administrative aspects of sponsored clinical trials, including subject recruitment, enrollment, and data collection. Acts as the primary liaison between sponsors and investigators while ensuring protocol adherence and regulatory compliance.
$31 - $46 / HOUR
2 days ago
Mass General Brigham
The coordinator manages clinical research studies on depression, focusing on participant recruitment, screening, and the administration of assessments. They are also responsible for data collection, maintaining regulatory binders, and contributing to scholarly manuscripts.
$29 / HOUR
Iterative Health
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.
Salary not listed
3 days ago
Mohawk Valley Health System
The Clinical Research Nurse facilitates and coordinates daily clinical trial activities, ensuring adherence to protocols and regulatory requirements. They work closely with the Principal Investigator to manage study documentation, participant recruitment, and data collection.
$75,000 - $115,000 / YEAR
4 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
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
Mid-Atlantic Permanente Medical Group PC
The Clinical Research Nurse coordinates the clinical trial study process, including patient recruitment, informed consent, and protocol-required assessments. They also ensure regulatory compliance by preparing IRB submissions and maintaining accurate study documentation throughout the lifecycle.
$79,370 - $99,213 / YEAR
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
Cedars-Sinai
The Clinical Research Coordinator independently manages study coordination, including patient screening, informed consent, and data collection. They ensure compliance with federal and local regulations while maintaining accurate source documents and reporting study progress.
$27 - $42 / HOUR
7 days ago
Vanderbilt University Medical Center
Coordinate clinical trial protocols, patient consent processes, and the preparation of IRB and regulatory documents. Identify and recruit research subjects while managing data collection and lab specimen shipping.
Vail Health Hospital
The Clinical Research Coordinator manages clinical trials by ensuring patient safety, regulatory compliance, and accurate data collection. They coordinate patient recruitment, maintain study documentation, and facilitate communication between investigators, sponsors, and clinical staff.
$32 - $44 / HOUR
8 days ago
TriHealth
Acts as a liaison between study sponsors, investigators, and the IRB to coordinate and conduct clinical research studies. Responsible for enrolling subjects, collecting data, and ensuring all research activities comply with IRB and FDA standards.
Headlands Research
Support clinical trial delivery by preparing study documents, conducting patient procedures like vital signs and phlebotomy, and managing study data. Coordinate participant visits and ensure compliance with FDA and Good Clinical Practice guidelines.
10 days ago
The role involves supporting clinical trial visits by performing phlebotomy, collecting patient vitals, and managing biological samples. Additionally, the assistant handles study documentation, data entry into EDC/CTMS systems, and general administrative support for research coordinators.
Support clinical trials by preparing study documents, recruiting participants, and conducting patient-facing procedures like vital signs and phlebotomy. Manage study data entry in EDC and CTMS systems while ensuring compliance with FDA and GCP guidelines.
$22 - $27 / HOUR
Coordinate all aspects of assigned clinical trials from site initiation through close-out while ensuring patient safety and data quality. Maintain strict compliance with protocols, FDA regulations, and GCP/ICH guidelines through accurate documentation and reporting.
$72,000 - $85,000 / YEAR
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
University of Miami
The Clinical Research Nurse 1 ensures the integrity and quality of clinical research studies by conducting them in accordance with federal and institutional regulations. They also play a key role in participant recruitment, data collection, and patient education throughout the study process.
11 days ago
