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Duke Careers
Overview
The specialist will support clinical research operations by managing participant documentation, data collection, and regulatory compliance for cancer studies. They will also collaborate with investigators to facilitate participant recruitment, study visits, and the preparation of research materials.
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Compensation
$21 - $31 / HOUR
Posted
13 days ago
ProHEALTH Medical Management
The Staff Nurse is responsible for the overall assessment, planning, implementation, and evaluation of patient care. This includes providing clinical nursing care and ensuring compliance with established regulations and standards.
Salary not listed
14 days ago
ICON plc
The Clinical Research Nurse provides direct clinical care to research participants and administers investigational products while monitoring safety. They also coordinate study procedures, ensure protocol compliance, and maintain accurate documentation of research data.
17 days ago
University of Texas Medical Branch (UTMB)
Coordinate and monitor all phases of research programs, including managing the National Laboratory Containment group and assisting the Community Liaison Committee. Perform data analysis, manage IRB documentation, and support the Principal Investigator with grant proposals and budget development.
25 days ago
Coordinate and monitor all phases of research programs, including managing the National Laboratory Containment group and the Community Liaison Committee. Perform data analysis, manage IRB documentation, and assist the Principal Investigator with grant proposals and budget development.
University of Oklahoma
The Research Coordinator will plan, design, conduct, and analyze scientific experiments within the Health Promotion Research Center. They are responsible for maintaining study accuracy and ensuring research procedures run smoothly in a collaborative environment.
$38,700 - $50,300 / YEAR
1 month ago
University of Chicago
The Clinical Research Coordinator I coordinates all aspects of conducting clinical trials, including screening, enrollment, and subject follow-up. They ensure compliance with Standard Operating Procedures and maintain accurate documentation throughout the study.
$50,000 - $65,000 / YEAR
University of California, Irvine
The Assistant Clinical Research Coordinator supports cancer-related clinical trials by managing data, coordinating protocol requirements, and assisting the Principal Investigator with patient recruitment and screening. They also serve as a liaison between sponsors, regulatory agencies, and the research team to ensure compliance with institutional and federal policies.
University of Rochester
The Outcomes Specialist supports research projects by coordinating study activities, managing participant recruitment, and conducting patient interviews. They also analyze research data, prepare study proposals, and disseminate findings through publications and presentations.
$23 - $32 / HOUR
Johns Hopkins University
The Research Program Coordinator manages daily logistical and operational activities for clinical research studies, including participant recruitment, enrollment, and data integrity. They also serve as a liaison between clinical staff, investigators, and community partners while ensuring adherence to study protocols and regulatory requirements.
$17 - $30 / HOUR
Cedars-Sinai
The Clinical Research Associate I coordinates clinical study implementation, abstracts research data, and ensures compliance with federal and institutional regulations. They are responsible for completing case report forms, managing regulatory submissions to the IRB, and assisting with patient research billing.
$24 - $33 / HOUR
Washington University in St. Louis
The Clinical Research Coordinator II manages complex clinical research activities, ensuring regulatory compliance and data integrity under the direction of the Principal Investigator. Responsibilities include coordinating study protocols, analyzing clinical data, and assisting in the preparation of manuscripts and grant proposals.
$52,600 - $78,900 / YEAR
St. Joseph Hospital & Medical Center
The Clinical Research Specialist manages clinical research studies by recruiting participants, obtaining informed consent, and ensuring protocol compliance. They act as a primary liaison between sponsors, investigators, and study subjects while maintaining accurate documentation and safety reporting.
$24 - $36 / HOUR
The role involves planning, coordinating, and implementing clinical research studies while ensuring adherence to regulatory guidelines and protocol standards. Responsibilities include managing participant enrollment, maintaining research records, and performing quality checks to ensure data accuracy and participant safety.
$25 - $35 / HOUR
The IIT Research Program Coordinator will manage investigator-initiated clinical trials from concept through activation and regulatory submission. They will collaborate with investigators, clinicians, and regulatory teams to ensure compliant and impactful research execution.
Penn State University
The coordinator will manage participant recruitment, screening, and data collection for clinical trials investigating dietary interventions. They will also handle visit scheduling and various research-related administrative tasks to support the lab's operations.
Mount Sinai Health System
The Clinical Research Assistant assists in daily research activities, including the collection and organization of study information. They also provide clerical support to coordinators and assist in the preparation of grant applications and regulatory documents.
$17 - $25 / HOUR
The Clinical Research Coordinator assists in daily research study activities, including obtaining informed consent and organizing study information. They also support the preparation of grant applications and regulatory documents for the Institutional Review Board.
2 months ago
UPMC
The Clinical Research Nurse coordinates oncology clinical trials by managing patient care, ensuring protocol compliance, and facilitating informed consent. They also collaborate with physicians and research staff to collect data and provide education to patients and their families.
Emory University
The Clinical Research Coordinator II manages research project databases, develops study-related documents, and ensures compliance with research protocols. They also interface with participants to determine eligibility, obtain consent, and supervise the collection and processing of study specimens.
