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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
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, 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
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
7 days ago
Headlands Research
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
9 days ago
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
Evolution Research Group
The Clinical Research Coordinator II manages the implementation and coordination of clinical trials, ensuring compliance with protocols and regulatory standards. They are responsible for subject recruitment, screening, informed consent, and maintaining accurate study documentation.
13 days ago
ProHEALTH Medical Management
The Clinical Research Coordinator is responsible for coordinating clinical trials, managing patient recruitment, and conducting patient visits. Key duties include handling IRB submissions, processing laboratory specimens, and ensuring strict adherence to study protocols and federal regulations.
$26 - $38 / HOUR
The Clinical Research Coordinator manages patient visits, recruitment, and the logistical aspects of clinical trials in accordance with regulatory standards. They are responsible for IRB submissions, data entry, and collaborating with physicians to ensure protocol adherence.
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
Ora
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks and collaborate with project managers and investigators to execute research directives.
