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Terumo
Overview
The Clinical Research Coordinator provides administrative and operational support to the Clinical Research and Operations department to ensure adherence to study plans and regulatory standards. Responsibilities include managing study documentation, maintaining the electronic trial master file, and coordinating with clinical sites and vendors.
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Compensation
$44,900 - $61,710 / YEAR
Posted
7 days ago
Dominion Diagnostics LLC
The Sample Preparation Scientist is responsible for preparing urine and oral fluid samples for drug confirmation testing using LC-MS/MS technology, which involves organizing and processing samples using robotic liquid handling instrumentation. Duties also include preparing necessary reagents and ensuring proper handling and documentation of all patient samples.
$45,000 - $50,000 / YEAR
16 days ago
North Coast Medical, Inc.
The Senior Quality Associate supports the execution and coordination of Quality Management System activities, handling administrative and technical support for document control, training, quality event tracking, and supplier controls within the electronic QMS. This role also independently manages low-risk quality events and complaint records while developing competency in investigations and regulatory compliance.
$27 - $30 / HOUR
3 months ago
Profound Research
The Assistant Clinical Research Coordinator supports clinical trial execution by assisting with patient recruitment, data collection, and ensuring regulatory compliance under the direction of site management and senior staff. Daily activities may include phlebotomy, laboratory tasks, data entry, and administrative assignments while adhering strictly to study protocols.
Salary not listed
The Assistant Clinical Research Coordinator supports clinical trial execution by assisting with patient recruitment, data collection, and regulatory compliance under the direction of site management and senior staff. This includes performing clinical trial activities such as phlebotomy, laboratory tasks, and data entry according to established research protocols.
Eurofins
Clinical Laboratory Scientists perform clinical laboratory procedures and examinations requiring independent judgment, ensuring adequate supervision of technicians and trainees based on workload demands. Responsibilities range from following standard operating procedures for specimen handling and equipment maintenance (Level I) to advanced troubleshooting and training (Levels II and III).
Clinical Laboratory Scientists perform clinical laboratory procedures and examinations requiring independent judgment, including operating, calibrating, and maintaining laboratory equipment according to standard operating procedures. They are also responsible for quality control, documenting corrective actions, training other technicians, and participating in process improvement projects.
Clinical Laboratory Scientists perform clinical laboratory procedures and examinations requiring independent judgment, ensuring sufficient staffing levels to meet workload demands and supervising technicians and trainees. Responsibilities range from basic specimen handling, equipment maintenance, and quality control documentation (Level I) to advanced troubleshooting, training, and participation in process improvement projects (Levels II and III).
Clinical Laboratory Scientists perform clinical laboratory procedures and examinations requiring independent judgment, ensuring adequate supervision of technicians and trainees. Responsibilities include operating, calibrating, and maintaining laboratory equipment, adhering to quality control policies, and documenting all corrective actions when test systems deviate from acceptable performance.
Clinical Laboratory Scientists perform clinical laboratory procedures and examinations requiring independent judgment, ensuring adequate supervision of technicians and trainees. Responsibilities include operating, calibrating, and maintaining laboratory equipment, adhering to quality control policies, and documenting all testing activities and corrective actions.
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.
