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The US Oncology Network
Overview
The Clinical Research Nurse identifies and screens patients for clinical trials and manages the informed consent process. They provide care for patients receiving investigational treatments and ensure accurate documentation of trial data.
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Compensation
Salary not listed
Posted
5 days ago
Tulane University
Coordinate day-to-day operations of cardiovascular disease studies and act as a liaison between patients, investigators, and sponsors. Responsible for screening and enrolling patients, ensuring protocol compliance, and maintaining regulatory documentation.
6 days ago
The Clinical Research Nurse manages patients receiving cutting-edge oncology treatments and coordinates clinical trial participation. Key duties include screening patients, conducting informed consent, and ensuring accurate trial documentation.
9 days ago
Urology of Indiana LLC
The Clinical Research Coordinator manages and documents clinical trials while ensuring adherence to GCP and FDA guidelines. Responsibilities include recruiting subjects, performing clinical assessments, and maintaining scientific data integrity.
13 days ago
The Clinical Research Nurse manages oncology patients throughout their journey by screening for clinical trials and conducting the informed consent process. They are responsible for administering investigational products, assessing adverse events, and ensuring accurate trial documentation.
1 month ago
DERMCARE MANAGEMENT LLC
The Clinical Research Coordinator is responsible for overseeing clinical trials, performing visit procedures such as phlebotomy and EKGs, and ensuring adherence to GCP and FDA regulations. They also manage investigational medication, maintain detailed study records, and engage with research subjects and sponsors.
Profound Research
The Clinical Research Coordinator will manage all clinical trial activities under supervision, ensuring compliance with protocols, laws, and regulations. Key duties include leading trial implementation from start-up to follow-up, training staff, managing documentation, and reporting adverse events.
3 months ago
CenExel
The coordinator is responsible for managing all facets of clinical trials, ensuring strict adherence to ICH, GCP, protocol, and company guidelines from initiation through completion. This includes coordinating patient involvement, organizing research information, monitoring subjects, reporting adverse events, and performing required safety and efficacy assessments.
The coordinator is responsible for managing all phases of clinical trials, ensuring strict adherence to ICH, GCP, protocol, and company guidelines, from initiation through completion. This includes organizing research information, monitoring subjects, reporting adverse events, performing safety assessments, and assisting the Clinical Trial Manager with various operational aspects.
$30 - $38 / HOUR
The coordinator is responsible for managing all facets of clinical trials, ensuring strict adherence to ICH, GCP, protocol, and company guidelines from initiation through completion. This includes coordinating patient involvement, organizing research information, monitoring data quality, performing safety assessments, and assisting the Clinical Trial Manager with various oversight duties.
4 months ago
