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Sarasota Memorial Health Care System
Overview
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.
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Compensation
Salary not listed
Posted
11 days ago
UTHealth Houston
The Research Coordinator III manages clinical trials in Movement Disorders, overseeing participant recruitment, data collection, and regulatory compliance. They serve as a primary liaison between investigators, sponsors, and regulatory bodies to ensure study milestones are met.
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
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.
22 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.
23 days ago
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
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.
25 days ago
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
Coordinate and manage a portfolio of high-complexity clinical trials in Neurological Surgery, including investigator-initiated and industry-funded studies. Responsibilities include recruiting participants, managing regulatory documentation, and ensuring compliance with FDA and University policies.
City of Hope
The Clinical Research Nurse coordinates oncology clinical trials, managing everything from patient recruitment and informed consent to data collection and biospecimen handling. They ensure strict adherence to federal regulations, study protocols, and institutional SOPs to protect human subjects.
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
University of Rochester
Coordinates administrative and clinical activities for human subject research projects focusing on muscular dystrophy. Responsibilities include participant recruitment, regulatory document management, and overseeing data integrity for clinical trials.
$21 - $30 / HOUR
1 month ago
CentraState Healthcare System
The Research Nurse oversees and directs the clinical course of research participants in clinical trials under the direction of the principal investigator or manager, ensuring strict adherence to local and federal laws and regulations. Key duties involve study implementation, subject recruitment, enrollment, accurate documentation, and acting as the liaison between the sponsor and physician regarding protocol activities.
$48 - $82 / HOUR
Montefiore Health System
The Research Associate supports the conduct of cancer clinical trials by managing patient data collection and ensuring protocol compliance. Key duties include obtaining informed consent, administering questionnaires, and coordinating study visits and specimen shipments.
$56,000 - $70,000 / YEAR
UCSF
Execute and coordinate clinical research protocols in the Department of Neurology, managing data collection and specimen management across multiple sites. Responsibilities include maintaining regulatory documents, managing IRB submissions via the CHR system, and ensuring compliance with institutional and agency policies.
$38 / HOUR
