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University of Texas Medical Branch (UTMB)New
Overview
Provides professional nursing care for participants in oncology and hematology research studies while ensuring compliance with study protocols and federal regulations. Manages clinical study operations, including participant recruitment, informed consent, data collection, and regulatory documentation.
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Compensation
Salary not listed
Posted
New
Provides professional nursing care for participants in oncology and hematology research studies while ensuring compliance with study protocols and federal regulations. Manages clinical study operations, including participant recruitment, data collection, and regulatory documentation.
Children’s Hospital of Philadelphia
This role coordinates clinical research activities, including managing day-to-day study operations and adhering to IRB-approved protocols. Key duties involve recruiting participants, maintaining regulatory documents, and ensuring patient safety and compliance.
$56,890 - $71,110 / YEAR
15 days ago
M3USA
The Clinical Research Assistant supports daily clinical trial activities, ensuring protocol compliance and data quality under the guidance of site leadership. Key duties include managing clinical supplies, performing phlebotomy, and documenting participant data in source records and EDC systems.
17 days ago
The Clinical Research Coordinator manages daily clinical trial activities and supports the Principal Investigator in the conduct of studies. Key duties include screening participants, maintaining documentation, and ensuring compliance with research protocols and laws.
$30 - $40 / HOUR
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the Investigator with participant screening, maintaining documentation, collecting and entering data, and overseeing other research staff.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting investigators with participant screening, maintaining documentation, mentoring staff, and ensuring all activities comply with research protocols and regulations.
University of Chicago
Coordinates and conducts complex clinical research studies while ensuring compliance with federal and institutional regulations. Acts as a key liaison between investigators, sponsors, and university departments to manage study documentation and operational workflows.
$60,000 - $75,000 / YEAR
18 days ago
The Clinical Research Coordinator manages daily clinical trial activities, including screening participants and maintaining essential study documentation. They ensure all activities comply with research protocols, laws, and regulatory requirements while supporting the Principal Investigator.
$25 - $35 / HOUR
21 days ago
University Hospitals
The therapist performs pulmonary function tests and manages subject scheduling to support clinical research studies. Responsibilities include executing protocols such as DLCO and 6mwt, maintaining research logs, and collaborating with coordinators to align tests with patient visits.
24 days ago
Washington University in St. Louis
Coordinates and implements cardiology research studies, including data collection and management of study protocols. Provides direct patient care, screens and enrolls subjects, and ensures compliance with IRB and regulatory requirements.
$56,200 - $96,100 / YEAR
25 days ago
This role coordinates and implements research studies, managing data collection while ensuring continuity of patient care and protection of human subjects under the Principal Investigator's guidance. Responsibilities include providing direct patient care, administering study interventions and medications, processing specimens, and collaborating with multidisciplinary teams and sponsors.
1 month ago
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with participant screening, maintaining documentation, and ensuring all activities comply with the research protocol and regulations.
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening participants, maintaining documentation, and ensuring compliance with research protocols.
Caris Life Sciences
Provide operational and regulatory support for sponsored and collaborative pharma studies, focusing on site onboarding and engagement. Manage study documentation, specimen tracking, and inventory while ensuring compliance with SOPs.
Coordinates and implements cardiology research studies, including data collection, patient screening, and enrollment. Manages protocol requirements, regulatory submissions to the IRB, and the administration of investigational products.
The Clinical Research Coordinator I facilitates daily clinical research activities, including participant screening, enrollment, and data collection. They ensure study compliance with federal and institutional regulations while maintaining accurate documentation and coordinating patient schedules.
$50,000 - $65,000 / YEAR
