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Nira Medical
Overview
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.
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Compensation
Salary not listed
Posted
9 days ago
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
13 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.
14 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.
15 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.
16 days ago
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
20 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.
21 days ago
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.
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
Genesis Orthopedics & Sports Medicine
Coordinate and manage clinical trials from startup to closeout, including participant recruitment, screening, and visit conduction. Maintain accurate study data, regulatory binders, and ensure strict adherence to GCP and protocol requirements.
28 days ago
IRONWOOD PHYSICIANS,P.C.
Manages and coordinates all clinical and administrative aspects of conducting clinical trials in accordance with protocol guidelines and federal regulations. Acts as a liaison between investigators, sponsors, and the IRB while performing patient procedures and assessments.
Washington University in St. Louis
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.
$56,200 - $96,100 / YEAR
29 days ago
UnityPoint Health
The research nurse manages all aspects of clinical trials, acting as a liaison between investigators, the IRB, and sponsors. Key duties include screening and enrolling subjects, ensuring protocol compliance, and maintaining accurate regulatory and data documentation.
Cincinnati Eye Institute
The Clinical Research Coordinator oversees study protocols, ensures regulatory compliance, and manages site activities including patient recruitment and data documentation. They also coordinate with sponsors, manage study budgets, and perform study-specific testing and exams according to protocol guidelines.
1 month ago
