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Duke Careers
Overview
Coordinate and manage oncology clinical trials, including study start-up, recruitment, and long-term follow-up for breast and gynecologic studies. Provide direct clinical nursing care to research participants, including chemotherapy administration and adverse event monitoring.
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Compensation
$64,966 - $104,996 / YEAR
Posted
15 days ago
K2 Staffing LLC
The Psychometric Rater is responsible for administering and interpreting tests as part of a clinical team investigating pharmaceutical treatments. This includes conducting assessments, maintaining documentation, and ensuring compliance with guidelines.
Salary not listed
17 days ago
ICON plc
The Senior CRA is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They also collaborate with site staff and contribute to the preparation of study documentation and clinical study reports.
The Clinical Research Associate is responsible for conducting site qualification, monitoring, and close-out visits to ensure protocol compliance and patient safety. They also collaborate with site staff to facilitate study conduct and perform data review to maintain high-quality clinical data.
25 days ago
University of Pennsylvania
Coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
1 month ago
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and data integrity. Additionally, you will collaborate with site staff and investigators to facilitate study conduct and maintain high-quality clinical data.
UVA Health
The Clinical Research Coordinator will recruit, screen, and enroll study participants while managing clinical trial data and documentation. They will also process laboratory specimens and maintain close communication with Principal Investigators and study sponsors.
St. Joseph Hospital & Medical Center
The Clinical Research Specialist manages clinical research studies by recruiting participants, obtaining informed consent, and ensuring protocol compliance. They act as a primary liaison between sponsors, investigators, and study subjects while maintaining accurate documentation and safety reporting.
$24 - $36 / HOUR
Quest Diagnostics
The Clinical Development Specialist oversees all operational aspects of clinical studies, including site selection, study initiation, documentation, and data monitoring. They also manage site payments, query resolution, and the flow of specimens while coordinating with internal and external stakeholders.
$57,475 - $103,455 / YEAR
CenExel
The Lab Technician will perform laboratory procedures, process clinical samples according to protocol, and maintain accurate inventory and harvest logs. They are also responsible for monitoring storage temperatures and ensuring all study materials are properly labeled and stored.
$20 - $21 / HOUR
Lurie Children's Hospital
The Behavioral Research Coordinator II manages multi-site HIV prevention and treatment trials, overseeing study operations from start-up to close-out. They are responsible for participant recruitment, regulatory documentation, data collection, and the delivery of behavioral interventions.
$49,920 - $81,619 / YEAR
VENTRE MEDICAL ASSOCIATES
The Clinical Research Coordinator facilitates and coordinates daily clinical trial activities, ensuring compliance with protocols and regulations. They assist the Principal Investigator in recruiting patients and managing study documentation.
5 months ago
