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Baylor Scott & White Health
Overview
The Research Nurse II coordinates clinical trials by managing protocols, screening patients for eligibility, and ensuring compliance with federal and institutional guidelines. They also collaborate with Principal Investigators and other departments to handle study documentation and data analysis.
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Compensation
Salary not listed
Posted
3 days ago
The Clinical Research Coordinator 2 supports Principal Investigators in conducting clinical trials from pre-study implementation to closure. Key duties include managing IRB reports, developing study budgets, and coordinating protocols across various departments.
8 days ago
The Christ Hospital Health Network
The Clinical Research Coordinator supports the Principal Investigator by coordinating daily clinical trial activities and ensuring data integrity. They provide guidance on compliance, financial, and personnel aspects of the study to ensure human subject safety.
10 days ago
The Research Nurse II coordinates clinical trials from setup to closure, ensuring adherence to federal and institutional guidelines. Key duties include screening patients for eligibility, managing informed consent, and collaborating with Principal Investigators and pharmacy staff.
11 days ago
Community Health Network
The Clinical Research Specialist develops and implements recruitment strategies to enroll patients in clinical trials. They are responsible for screening patients, managing data entry, and ensuring compliance with protocol and regulatory standards.
17 days ago
The Clinical Research Specialist develops and implements recruitment strategies to enroll patients in clinical trials. They are responsible for screening patients, facilitating feasibility reviews, and ensuring data entry complies with protocol and regulatory standards.
University of Colorado
Coordinate day-to-day operations of clinical trials, including patient recruitment, informed consent, and data collection. Ensure strict adherence to FDA and regulatory standards while collaborating with investigators and hospital staff.
$49,899 - $58,705 / YEAR
22 days ago
Coordinate day-to-day operations of clinical trials, including patient recruitment, informed consent, and data recording in CRFs. Collaborate with investigators and hospital staff to ensure protocol compliance and manage sponsor monitor visits.
Southcoast Health System, Inc.
Coordinate all activities related to clinical trials, including patient screening, follow-up, and correspondence with the Institutional Review Board and sponsors. Manage trial implementation, budget negotiations, and ensure strict adherence to federal and institutional guidelines for human subject research.
$57,554 - $96,762 / YEAR
24 days ago
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.
$55,962 / YEAR
29 days ago
The Clinical Research Associate manages patient recruitment, registration, and scheduling while providing clerical support to the research team. They are responsible for data entry, quality assurance, and maintaining study records to ensure protocol adherence.
$63,336 / YEAR
1 month ago
The Clinical Research Nurse coordinates and oversees clinical research operations for assigned trials while ensuring compliant patient care. They act as a liaison between investigators and regulatory bodies, manage study documentation, and monitor patient progress throughout the clinical trial process.
$106,330 / YEAR
2 months ago
Veterinary Emergency Care, PLLC
The Rehabilitation Therapist will be responsible for performing patient assessments and executing individualized treatment plans while delivering high-quality, hands-on rehabilitation therapies. This role also requires clear communication with doctors, clients, and team members, alongside maintaining accurate medical records to support a patient-first environment.
RCCA MSO LLC
The Research Coordinator serves as the primary point of contact for clinical trials, overseeing study procedures from start to finish. Responsibilities include patient recruitment, data management, regulatory documentation, and ensuring compliance with safety protocols and institutional guidelines.
$27 - $37 / HOUR
3 months ago
The Clinical Research Nurse coordinates and oversees clinical research operations for assigned trials, participating in assessing, planning, implementing, and evaluating compliant patient care within those trials under the principal investigator's supervision. Key duties include assisting with trial preparation, managing regulatory submissions to the IRB, recruiting and educating patients, monitoring patient progress, and maintaining accurate documentation.
$111,925 / YEAR
4 months ago
