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University of Massachusetts Medical SchoolNew
Overview
The Research Nurse Coordinator I manages complex research protocols, ensuring adherence to GCP standards and regulatory requirements. They act as a primary liaison between clinical partners, investigators, and sponsors while overseeing patient care and data integrity.
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Compensation
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Posted
New
University of Texas Medical Branch (UTMB)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, informed consent, data collection, and regulatory documentation.
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.
University of RochesterNew
The Clinical Research Nurse II is responsible for providing competent direct patient care and supporting unit activities to enhance care delivery. This includes performing patient care tasks, collaborating on care plans, and maintaining positive relationships with healthcare team members.
$35 - $46 / HOUR
Cleveland Clinic
The Research Nurse assists with the implementation and conduct of human subject research projects while ensuring adherence to protocols. Responsibilities include managing regulatory documents, monitoring patient safety, and coordinating care plans in collaboration with the research team.
3 days ago
The Research Nurse will assist patients, work on research trials, and perform various administrative tasks while supporting the GI research teams. Responsibilities include coordinating research projects, completing regulatory documents, and providing patient care based on research protocols.
Fortrea
The Research Nurse will deliver high-quality care to trial participants, monitor their well-being, and respond to emergencies while administering investigational compounds and performing study procedures like ECGs and venipuncture. Responsibilities also include collecting and processing biological samples and ensuring strict adherence and accurate record-keeping for clinical protocols.
The Research Nurse will assist in implementing and conducting human subject research projects, primarily focusing on critical care drug and device clinical trials, while ensuring strict adherence to research protocols. Key duties include managing regulatory documentation, developing data monitoring plans, reporting serious adverse events, and utilizing the nursing process for patient care and coordination.
As a Radiation Oncology Research Nurse, you will assist with the implementation and conduct of human subject research projects, ensuring adherence to research protocol requirements. This role involves direct patient interaction, coordination of clinical research trials, and administrative tasks related to study management.
Oversee the implementation and conduct of human subject research projects within the Heart, Vascular & Thoracic Institute. Perform nursing tasks including patient assessments, care plan development, documentation, and regulatory compliance.
4 days ago
OneOncology
As the Research Nurse, you will screen, enroll, and follow study subjects, ensuring protocol compliance and monitoring. You will also be responsible for source documentation, recording adverse events, and dispensing investigational products.
University of Iowa
Provide direct nursing care and administer investigational treatments for Phase I-IV clinical trials. Collaborate with medical staff to ensure participant safety and strict adherence to research protocols.
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
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
5 days ago
Weill Cornell Medical College
The Research Nurse Specialist ensures optimal quality of medical care for patients participating in clinical research studies and assists in the formation of educational materials. They also assess patient eligibility, coordinate informed consent, and monitor adherence to study protocols.
$108,972 - $125,388 / YEAR
The Research Nurse Specialist executes various technical and administrative tasks related to specific clinical research studies, ensuring optimal quality of medical care and ethical conduct for participating patients. Responsibilities include educating staff on drug protocols, assisting with policy updates, and managing study documentation and specimen handling according to protocol.
The Research Nurse Specialist is responsible for ensuring the optimal quality of medical care for patients enrolled in clinical research studies while maintaining ethical conduct. This includes assisting with the creation of educational materials for patients and staff, and educating nursing staff on drug protocols.
The Research Nurse Specialist ensures optimal quality of medical care and ethical conduct for patients in clinical research studies, assisting with educational materials and staff training on drug protocols. Responsibilities include assessing patient eligibility, managing follow-up visits, implementing interventions for adverse responses, and coordinating necessary laboratory work and scans.
The Research Nurse Specialist ensures optimal quality of medical care and ethical conduct for patients in clinical research studies, while also assisting in creating educational materials for patients and staff. Responsibilities include assessing patient eligibility, managing study drug monitoring, performing necessary laboratory procedures, and coordinating follow-up visits.
TriHealth
Acts as a liaison between study sponsors, investigators, and the IRB to coordinate and conduct clinical research studies. Responsible for enrolling subjects, collecting data, and ensuring all research activities comply with IRB and FDA standards.
8 days ago
