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Mid-Atlantic Permanente Medical Group PC
Overview
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.
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Compensation
$79,370 - $99,213 / YEAR
Posted
4 days ago
Terumo
The Clinical Research Coordinator provides administrative and operational support to the Clinical Research and Operations department to ensure adherence to study plans and regulatory standards. Responsibilities include managing study documentation, maintaining the electronic trial master file, and coordinating with clinical sites and vendors.
$44,900 - $61,710 / YEAR
7 days ago
Mercyhealth Wisconsin and Illinois
The Clinical Research Coordinator is responsible for recruiting and consenting study participants, managing regulatory documentation, and ensuring protocol adherence. They also handle specimen collection and processing while maintaining accurate data submission and reporting adverse events.
$27 - $42 / HOUR
9 days ago
Baylor Scott & White Health
The Research Nurse II coordinates clinical trials from setup to closure, ensuring adherence to federal and institutional guidelines. Key duties include screening patients for eligibility, managing informed consent, and collaborating with Principal Investigators and pharmacy staff.
Salary not listed
10 days ago
Sarasota Memorial Health Care System
Responsible for the timely and accurate administration of regulatory compliance for clinical research, including processing Human Research Protection Program and IRB documentation. The role involves informing leadership and staff regarding the regulatory status of clinical trials.
11 days ago
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
University of Texas Medical Branch (UTMB)
The coordinator obtains human subject data according to study protocols and manages general administrative duties to support clinical research. Key tasks include recruiting participants, maintaining regulatory documentation, and processing laboratory specimens.
16 days ago
The coordinator obtains human subject data according to study protocols and performs administrative duties to support clinical research. Key tasks include recruiting participants, managing regulatory documentation, and processing laboratory specimens.
SerenaGroup Inc
The Clinical Research Coordinator manages day-to-day clinical trial activities, including patient recruitment, screening, and study visit execution. They are responsible for maintaining accurate study documentation and ensuring compliance with FDA and ICH-GCP guidelines.
20 days ago
Providence
Coordinates and maintains diverse activities for neurology clinical research trials, ensuring protocol adherence and timely study completion. Acts as a liaison for regulatory documents and manages subject recruitment, informed consent, and study documentation.
$32 - $49 / HOUR
22 days ago
UT Southwestern Medical Center
Coordinate a portfolio of high-complexity neurological surgery trials, including investigator-initiated and industry-funded studies. Manage regulatory compliance, subject recruitment, data collection, and patient safety monitoring according to protocol guidelines.
23 days ago
Coordinate a portfolio of high-complexity neurological surgery trials, including investigator-initiated and industry-funded studies. Manage regulatory compliance, subject recruitment, data collection, and the execution of study procedures according to protocol.
Cedars-Sinai
Coordinates clinical research studies for kidney transplants, including patient screening, informed consent, and data collection. Ensures strict compliance with FDA, IRB, and GCP guidelines while managing study documentation and reporting.
$24 - $40 / HOUR
McLaren Health Care
Facilitates clinical research studies by evaluating candidate eligibility and managing the informed consent process. Coordinates study procedures, collects data, and ensures compliance with research protocols and regulatory requirements.
Oregon Health & Science University
The Senior Clinical Research Assistant manages patients on clinical trials, including consenting, enrolling, and gathering data. They are also responsible for regulatory tasks, sample processing, and assisting the Clinical Research Manager with various projects.
$48,734 - $77,522 / YEAR
24 days ago
Main Line Health
Manage a variety of cardiovascular device trials and support Phase II-IV drug studies. Coordinate study procedures according to protocols while collaborating with physician investigators and clinical teams.
St. Luke's University Health Network
The coordinator is responsible for the screening, enrollment, and coordination of clinical trials while ensuring compliance with protocol and federal regulations. Key duties include managing study documentation, performing study procedures, and coordinating data collection across departments.
The US Oncology Network
The coordinator is responsible for screening and enrolling patients in clinical trials, managing protocol compliance, and coordinating patient care. They also handle data collection, regulatory documentation, and the administration of investigational drugs.
25 days ago
Ochsner Health
This role manages and executes clinical trial activities, including patient recruitment, screening, and the administration of investigational therapies. The researcher serves as a liaison between patients and principal investigators while ensuring strict adherence to Good Clinical Practice guidelines.
Coordinate and manage a portfolio of high-complexity clinical trials within the Department of Neurological Surgery. Responsibilities include managing regulatory documentation, recruiting participants, and ensuring compliance with FDA and University policies.
28 days ago
