Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
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.
Quick view →
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
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
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.
24 days ago
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.
University of New Mexico
Coordinate and manage regulatory compliance and documentation for pediatric oncology/hematology clinical research studies. Facilitate trial start-up and maintenance while providing technical assistance to research staff on IRB and regulatory requirements.
$3,845 - $5,399 / MONTH
1 month ago
University of Rochester
Coordinates all aspects of human subject research studies within the Cerebrovascular and Neurocognitive Research Group, including recruitment, enrollment, and study visit execution. Manages regulatory requirements, IRB submissions, and mentors junior research coordinators to ensure protocol compliance.
$25 - $35 / HOUR
Carilion Clinic
The Clinical Research Coordinator supports cardiology clinical trials by managing administrative activities, recruiting participants, and ensuring compliance with regulatory guidelines. They serve as a liaison between sponsors, IRBs, and medical staff while mentoring junior coordinators and assisting in grant writing.
Hoag
The Clinical Research Coordinator RN manages all aspects of FDA-regulated clinical trials, from protocol review and subject recruitment to data collection and regulatory maintenance. They work closely with study physicians to ensure the accurate execution of Phase I-IV trials and maintain compliance with Good Clinical Practices.
$49 - $76 / HOUR
The role involves screening and enrolling patients for cellular therapy trials and managing the informed consent process. Additionally, the nurse maintains regulatory documents and collaborates with physicians to ensure protocol compliance and patient safety.
Children’s Minnesota
The Clinical Research Coordinator serves as a project manager to coordinate and implement neonatal research studies while ensuring compliance with protocols and regulatory requirements. Responsibilities include managing study activities, preparing regulatory submissions, overseeing data collection, and facilitating communication between investigators and stakeholders.
Jefferson Health Plans
Oversee the day-to-day activities of clinical trials from startup to closeout in accordance with Good Clinical Research Practice. Ensure study procedures, data management, and regulatory documentation meet protocol requirements and institutional standards.
The Clinical Research Coordinator screens and enrolls patients in clinical trials while ensuring strict compliance with study protocols and regulatory standards. They also collaborate with physicians to monitor patient conditions, manage investigational drugs, and maintain accurate research documentation.
The Human Subject Research Specialist II coordinates clinical trial activities, including participant enrollment, protocol implementation, and data management within the infectious disease division. They ensure compliance with regulatory standards, maintain research records, and assist with quality assurance audits.
The Clinical Research Coordinator manages the screening, enrollment, and monitoring of research patients within a clinical setting. They are responsible for maintaining study documentation, processing patient specimens, and ensuring compliance with IRB and regulatory requirements.
Cancer Care Associates of York
The Clinical Research Nurse ensures the integrity and quality of clinical research by implementing recruitment procedures and maintaining compliance with study protocols. They also provide direct patient care, including data collection, specimen processing, and monitoring patient responses to investigational agents.
MAPMG
The Clinical Research Nurse coordinates the clinical trial study process, including patient recruitment, informed consent, and protocol-required procedures. They also ensure regulatory compliance, maintain accurate study documentation, and monitor patient outcomes throughout the study lifecycle.
This entry-level exempt position coordinates the screening, enrollment, and maintenance of patients participating in clinical trials, ensuring strict adherence to protocol compliance and Good Clinical Practice (GCP). Key duties involve collaborating with providers on patient assessments, managing investigational drug accountability, accurate documentation, and participating in staff and patient education.
2 months ago
