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Professional Case ManagementNew
Overview
The Certified Mobile Research Nurse is responsible for scheduling and conducting mobile visits for pediatric study participants. They must perform physical assessments, collect specimens, and submit accurate source documentation in coordination with project managers.
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Compensation
$65 / HOUR
Posted
New
Visionary Ophthalmology
The coordinator manages day-to-day activities for ophthalmology clinical trials, including subject visits and regulatory compliance. They are responsible for data entry, maintaining study binders, and communicating with sponsors and CROs.
$25 - $30 / HOUR
9 days ago
Nira Medical
Perform clinical duties including vital signs, blood draws, and ECGs while managing laboratory specimens. Responsible for accurate data entry into EDC systems and ensuring compliance with GCP, IRB, and HIPAA regulations.
Salary not listed
Inova
The coordinator manages study operational activities in compliance with Good Clinical Practice and regulatory standards. Responsibilities include explaining investigational product processes, performing study tasks, and managing communication channels for research results.
Adams Clinical
Provide foundational operational and administrative support for clinical trials, including participant screening, scheduling, and clinical procedures. Maintain accurate ALCOA+-compliant documentation and perform data entry into EDC systems to ensure audit readiness.
$22 - $25 / HOUR
14 days ago
The Enrollment RA supports the evaluation, triage, and enrollment of clinical trial participants while ensuring compliance with study protocols and regulatory requirements. They perform essential administrative and clinical tasks, including scheduling, data entry, and basic clinical procedures like vital signs and phlebotomy.
$18 - $24 / HOUR
Ora
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks and collaborate with project managers and investigators to execute research directives.
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks, manage study documentation, and collaborate with investigators to execute research directives.
Iterative Health
The Clinical Research Coordinator II manages daily clinical trial activities, including protocol management, patient recruitment, and study visit coordination. They are responsible for ensuring data integrity, maintaining regulatory documentation, and serving as the primary point of contact for study participants.
15 days ago
The Senior Clinical Research Coordinator manages daily clinical trial activities, including patient recruitment, protocol adherence, and clinical procedures. They also ensure accurate data entry, maintain study documentation, and coordinate with sponsors and investigators to meet enrollment targets.
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.
Care Access
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
$60,000 - $90,000 / YEAR
21 days ago
Tandem Intermediate LLC
The Clinical Research Assistant supports daily clinic operations and ensures study procedures are followed according to protocol guidelines. Key duties include collecting and processing laboratory samples, screening patients, and maintaining regulatory documentation.
The Clinical Research Assistant supports daily clinical research activities, ensuring strict adherence to study protocols and managing patient visits. Key duties include collecting and processing laboratory specimens, performing clinical tasks like phlebotomy, and maintaining accurate regulatory documentation.
The Clinical Research Nurse oversees daily study activities and ensures all procedures follow protocol guidelines. Responsibilities include collecting patient data, performing clinical tasks, and maintaining communication between investigators, sponsors, and patients.
MyMichigan Health
The Clinical Research Nurse provides direct patient care to study participants while ensuring strict adherence to research protocols and regulatory guidelines. They coordinate study activities, manage data collection, and act as a liaison between investigators, sponsors, and participants.
22 days ago
Sanford Health
Organize and coordinate complex components of clinical trials, including patient recruitment, screening, and the administration of investigational treatments. Maintain accurate study documentation, resolve data queries, and collaborate with physician investigators to ensure protocol compliance.
$24 - $39 / HOUR
23 days ago
Alcanza Clinical Research
The Clinical Research Nurse ensures the execution of assigned studies by performing clinical procedures and managing patient follow-up visits. Responsibilities include documenting in source charts, entering data into EDC, and maintaining compliance with FDA and GCP regulations.
Tulane University
Coordinate day-to-day operations for cardiovascular disease studies, acting as a liaison between patients, investigators, and sponsors. Responsibilities include screening and enrolling patients, ensuring protocol compliance, and managing regulatory documentation.
27 days ago
