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Duke Careers
Overview
This role involves managing all aspects of clinical research operations within the Anesthesiology Clinical Research Unit, including preparing FDA regulatory submissions, managing investigational products, and ensuring protocol compliance across various settings.
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Compensation
$59,829 - $99,960 / YEAR
Posted
13 days ago
CenExel
Oversee daily clinical study activities and serve as a liaison between the investigative site and the sponsor. Provide general nursing care to participants while ensuring accurate and ethical documentation of the research process.
$39 - $42 / HOUR
14 days ago
Pinnacle Clinical Research
The Clinical Research Coordinator manages daily clinical trial operations, including patient recruitment, screening, and study protocol execution. They ensure regulatory compliance, maintain accurate documentation, and collaborate with sponsors and medical staff to provide high-quality patient care.
Salary not listed
1 month ago
K2 Staffing LLC
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and ongoing reporting. They also collaborate with clinical operations, sponsors, and IRBs to ensure audit-ready regulatory files and compliance with study protocols.
2 months ago
INSIGHT Surgical Hospital
The Clinical Research Coordinator will support principal investigators, act as a liaison between sponsors and the institute, and oversee the details of clinical studies, ensuring compliance with review boards and regulations across multiple research projects. Key duties include providing technical support, directing trial operations, managing enrolled patients, maintaining regulatory documents, and reporting adverse events to all governing bodies.
3 months ago
The Clinical Research RN I oversees daily clinical study activities, acting as a liaison between the site and the Sponsor while ensuring accurate and ethical documentation throughout the research process. Essential duties include providing direct nursing care to participants, executing research protocols, screening subjects, and managing study documentation and supplies.
4 months ago
US Foot & Ankle Specialists
The Clinical Research Coordinator manages and conducts clinical research projects, leading trial operations, collecting data, and ensuring strict adherence to Foot and Ankle Specialists of the Mid-Atlantic (FASMA) Standard Operating Procedures (SOPs). Key duties include acting as a liaison between investigators, sponsors, and regulatory bodies, maintaining all required study documentation, and overseeing subject enrollment and data entry.
The coordinator assists in managing all aspects of patient involvement in clinical trials from initiation to completion, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. Key duties include organizing research information, observing subjects, scheduling data collection, documenting adverse events, and performing safety and efficacy assessments per protocol.
$29 - $33 / 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.
The Clinical Research Coordinator manages and conducts clinical research projects by leading trial operations, ensuring adherence to Standard Operating Procedures (SOPs), and acting as a liaison between investigators, sponsors, and regulatory bodies. Key duties include monitoring study activities, maintaining detailed records, managing subject enrollment, and handling adverse event reporting.
The coordinator is independently responsible for managing all phases of multiple or complex clinical trials, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. Key duties include coordinating patient involvement, organizing research information, monitoring study schedules, reporting adverse events, and managing research data quality.
$35 - $41 / HOUR
5 months ago
