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UVA HealthNew
Overview
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary research teams to support the advancement of cancer research.
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Compensation
$28 - $81,500 / HOUR
Posted
New
Veterinary Practice Partners
Design and implement individualized rehabilitation plans for canine patients using advanced therapeutic techniques like hydrotherapy and laser therapy. Collaborate with the medical team and pet families to monitor progress and adjust treatment plans to ensure optimal recovery and mobility.
$70,000 - $120,000 / YEAR
3 days ago
Independence Veterinary Clinic
Design and lead individualized rehabilitation plans for canine patients recovering from surgery or managing chronic conditions. Deliver hands-on therapies including hydrotherapy, therapeutic laser, and manual techniques while partnering with pet families to track progress.
University of Virginia
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring ethical and regulatory compliance. Manage study visits, collect high-quality data, and maintain accurate documentation while collaborating with multidisciplinary research teams.
$32 / HOUR
7 days ago
The coordinator will recruit, screen, consent, and enroll participants in oncology clinical trials while building relationships with patients and collecting high-quality data at study visits. Key duties involve maintaining accurate documentation, processing lab specimens, tracking adverse events, and ensuring strict protocol and regulatory compliance.
$33 - $92 / HOUR
Nevada System of Higher Education
The Research Coordinator will recruit and screen clinical trial participants, manage regulatory documentation, and provide clinical care services including patient monitoring and sample processing. They will also assist with study budget proposals, data entry, and ensure adherence to institutional and federal protocols.
$25 - $37 / HOUR
8 days ago
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary teams to support the advancement of innovative cancer research.
9 days ago
The coordinator will recruit, screen, consent, and enroll participants across multiple cancer clinical trials while building relationships with study participants. Key duties include coordinating study visits, collecting high-quality data, maintaining accurate documentation, processing specimens, tracking adverse events, and ensuring protocol compliance.
$28 - $82 / HOUR
UTHealth Houston
The Research Coordinator III manages clinical trials in Movement Disorders, overseeing participant recruitment, data collection, and regulatory compliance. They serve as a primary liaison between investigators, sponsors, and regulatory bodies to ensure study milestones are met.
Salary not listed
11 days ago
ProHEALTH Medical Management
The Clinical Research Coordinator is responsible for coordinating clinical trials, managing patient recruitment, and conducting patient visits. Key duties include handling IRB submissions, processing laboratory specimens, and ensuring strict adherence to study protocols and federal regulations.
$26 - $38 / HOUR
13 days ago
The Clinical Research Coordinator manages patient visits, recruitment, and the logistical aspects of clinical trials in accordance with regulatory standards. They are responsible for IRB submissions, data entry, and collaborating with physicians to ensure protocol adherence.
UVA Health
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring high-quality data collection and protocol compliance. Collaborate with multidisciplinary teams to manage study visits, maintain accurate documentation, and process laboratory specimens.
$33 - $91,500 / HOUR
23 days ago
The coordinator will recruit, screen, consent, and enroll participants in oncology clinical trials, building relationships with patients while coordinating study visits and collecting high-quality data. Key duties involve maintaining accurate documentation, processing lab specimens, tracking adverse events, and ensuring strict protocol and regulatory compliance.
Highmark Health
The role involves planning and managing clinical trials while ensuring compliance with regulatory bodies and human subject research standards. Key duties include identifying eligible patients, providing education to staff and participants, and maintaining clinical data and regulatory binders.
29 days ago
Lehigh Valley Health Network
Supervises and performs inpatient and outpatient stress testing and physical fitness evaluations for high-risk cardiac patients. Collaborates with physicians to determine protocols and integrate testing data into final diagnostic reports.
1 month ago
Shriners Children's
The Clinical Research Coordinator II ensures oversight and compliance of clinical research activities while serving as the primary liaison between participants, investigators, and sponsors. They are responsible for ethically recruiting pediatric subjects, collecting data, and ensuring subject safety and data quality.
$27 - $41 / HOUR
UTHealth (University of Texas Health Science Center at Houston)
Coordinate and manage clinical trials in Movement Disorders, overseeing participant recruitment, data collection, and regulatory compliance. Serve as a liaison between investigators and sponsors while managing study documentation and reporting.
Franciscan Alliance, Inc.
The coordinator implements and completes clinical research protocols, including obtaining informed consent and performing protocol-specified procedures. They are responsible for recruiting subjects, maintaining documentation, and reporting adverse events to sponsors.
The Clinical Research Coordinator manages the initiation and completion of clinical trials while ensuring compliance with regulatory standards and patient safety. They interface with clinical staff and patients to provide education, obtain informed consent, and maintain accurate clinical data.
Hackensack Meridian Health
The Clinical Research Nurse coordinates and oversees clinical research operations for assigned trials, ensuring compliant patient care and regulatory adherence. Responsibilities include recruiting patients, managing informed consent, monitoring patient progress, and acting as a liaison between investigators and sponsors.
$113,610 / YEAR
