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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
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
Arizona Liver HealthNew
Coordinate clinical research trials by recruiting participants, performing clinical procedures like phlebotomy and vitals, and managing study data. Ensure strict adherence to regulatory guidelines, maintain study documentation, and collaborate with sponsors and internal staff.
$28 - $36 / HOUR
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.
Salary not listed
3 days ago
Ascension
Coordinate administrative and clinical aspects of multiple oncology research projects, including participant recruitment and monitoring. Collaborate with investigators and sponsors to ensure protocol compliance and manage IRB documentation and audits.
4 days ago
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
4 C Medical Technologies
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
$75,000 - $95,000 / YEAR
6 days ago
Cedars-Sinai
The Clinical Research Coordinator independently manages study coordination, including patient screening, informed consent, and data collection. They ensure compliance with federal and local regulations while maintaining accurate source documents and reporting study progress.
$27 - $42 / HOUR
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
University of Miami
The coordinator manages simple clinical research protocols, including participant pre-screening, enrollment, and data collection. They are also responsible for monitoring adverse events, ensuring regulatory compliance, and maintaining study-specific regulatory binders.
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
Vail Health Hospital
The Clinical Research Coordinator manages clinical trials by ensuring patient safety, regulatory compliance, and accurate data collection. They coordinate patient recruitment, maintain study documentation, and facilitate communication between investigators, sponsors, and clinical staff.
$32 - $44 / 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
Evolution Research Group
The Sub-Investigator provides clinical and medical oversight at the research site to ensure study protocols and regulatory standards are met. They are responsible for subject safety, data integrity, and collaborating with the Principal Investigator to manage clinical trial activities.
9 days ago
The Clinical Research Coordinator manages the overall implementation, organization, and coordination of clinical trials at the site. They are responsible for ensuring protocol adherence, managing subject recruitment, and maintaining accurate regulatory documentation under the direction of the Principal Investigator.
The Clinical Research Coordinator manages the implementation of clinical trials, ensuring adherence to protocols and regulatory requirements. They are responsible for screening and enrolling subjects, maintaining accurate study records, and reporting adverse events under the direction of the Principal Investigator.
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.
Headlands Research
The Clinical Research Coordinator will manage and execute Phase II-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaborating with investigators and lab teams to maintain study integrity.
Key responsibilities involve preparing and administering specialized therapies, including IV infusions, monitoring study participants, and thoroughly documenting all clinical activities to support operational and clinical objectives. The role also requires conducting intake procedures, performing cognitive assessments, and maintaining clear communication to ensure participant safety and protocol compliance.
