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Keck Medicine of USC
Overview
The technician provides routine laboratory support for immune monitoring and flow cytometry services. Key duties include processing human specimens, maintaining equipment, and preparing technical reports.
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Compensation
$25 - $27 / HOUR
Posted
11 days ago
AstraZeneca
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for sites, driving performance, resolving study-related issues, and managing study supplies.
$112,154 - $168,232 / YEAR
University of Southern California
Labcorp
Perform routine and complex technical laboratory procedures and maintain instrumentation to ensure accurate test results. Responsible for specimen processing, quality control documentation, and maintaining a safe work environment.
Salary not listed
28 days ago
The Medical Technologist will perform routine and complex laboratory testing, troubleshoot instrumentation, and ensure accurate reporting of results. They are also responsible for maintaining quality control, preventive maintenance, and a safe laboratory environment.
$32 - $49 / HOUR
1 month ago
The Medical Lab Technologist will perform routine and complex technical procedures in hematology, urinalysis, and coagulation while ensuring accurate test results. They are also responsible for maintaining laboratory instrumentation, performing quality control, and ensuring a safe work environment.
Montefiore Health System
The Research Associate supports the conduct of cancer clinical trials by managing patient data collection and ensuring protocol compliance. Key duties include obtaining informed consent, administering questionnaires, and coordinating study visits and specimen shipments.
$56,000 - $70,000 / YEAR
The Medical Lab Technologist is responsible for performing routine and complex technical procedures, operating laboratory instrumentation, and ensuring accurate test results. They must also maintain a safe work environment, perform quality control, and troubleshoot equipment to ensure proper functionality.
Profound Research
The Clinical Research Coordinator manages all clinical trial activities, including study start-up, subject recruitment, and data collection in compliance with protocols and regulations. They also mentor staff and ensure accurate documentation and reporting of adverse events.
The Clinical Research Coordinator manages all clinical trial activities, including study start-up, subject recruitment, and data collection in compliance with protocols. They also mentor staff and ensure accurate documentation and reporting of adverse events.
The Clinical Research Coordinator manages all clinical trial activities in compliance with study protocols, regulations, and company standards. They are responsible for subject recruitment, data collection, regulatory documentation, and mentoring staff to ensure high-quality clinical research operations.
The Clinical Research Coordinator manages all clinical trial activities in compliance with research protocols, regulations, and company standards. They are responsible for subject recruitment, data collection, regulatory documentation, and mentoring staff to ensure high-quality clinical trial conduct.
Medpace, Inc.
The Medical Writer will write IND and NDA modules, clinical study reports, protocols, and amendments. They will also coordinate quality control reviews and interact closely with sponsors and subject matter experts.
The Clinical Safety Coordinator will collect, process, and track serious adverse event reports while generating safety narratives and queries. They will also perform quality control of safety cases and collaborate with internal departments and clinical research sites to ensure compliance with safety processes.
The Clinical Trial Assistant will provide day-to-day support for Training & Development activities, including maintenance of files and scheduling training sessions. Additional responsibilities include conducting quality control reviews and supporting other departments on ad hoc projects.
The Clinical Safety Coordinator will collect, process, and track serious adverse event reports while generating safety narratives and performing quality control of safety cases. Collaboration with internal departments and clinical research sites is essential to ensure compliance with safety processes.
EMSL ANALYTICAL INC
The Laboratory Analyst II is responsible for the preparation and analysis of microbiological samples, including fungi, bacteria, and Legionella. They will also manage analytical reports, maintain laboratory equipment, and perform quality control practices.
$23 / HOUR
2 months ago
