Well established clinical research center looking for an experienced Clinical Research Coordinator to coordinate and implement the clinical studies, evaluate and abstract research data and ensure compliance with protocols and research objectives. This role is responsible for completing case report forms, entering clinical research data, assisting with regulatory submissions to the IRB including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines, preparing and shipping samples.
Job Details
ID | #51441310 |
Estado | California |
Ciudad | Los angeles |
Fuente | California |
Showed | 2024-04-10 |
Fecha | 2024-04-10 |
Fecha tope | 2024-06-09 |
Categoría | Salud |
Crear un currículum vítae |
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