- Cedars-Sinai (Los Angeles, CA)
- …budget and patient research billing. This role will comply with all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study and ... Clinical Research Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to coordinate and/or implement… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …calibration, maintenance, and OOT records to comply with ISO 13485, ISO 9001, and FDA regulations . + Provide input to the Calibration and Equipment Maintenance ... and department daily activities as a quality approver and coordinator . + Review and support Internal and External audits...preferred. + Knowledge of ISO 13485, ISO 9001, and FDA regulations is highly At BD, we… more
- Abbott (Sylmar, CA)
- …regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) regulations , other regulatory requirements, Company policies, operating ... RI audit readiness preparation. + Acts as change order coordinator for RI. + Supports SQEs pull and verify...reading and experience with inspection sampling techniques. Knowledge of FDA , GMP, ISO 13485. Good communication and computer skills,… more
- Cedars-Sinai (Los Angeles, CA)
- …Research Associate I/CPT works under the direction of a Clinical Research Coordinator , Research Program Administrator, Research Nurse, or other supervising staff to ... and Responsibilities** + Works under the direction of a Clinical Research Coordinator , Research Program Administrator, Research Nurse, or other supervising staff to… more
- Cedars-Sinai (Los Angeles, CA)
- …study budget and patient research billing. This role will follow all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study and ... lives. The CRA I member will work directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to coordinate and/or implement the… more
- Cordis (Irvine, CA)
- …(Coronary)** role is a key position within the coronary program to help ensure FDA clearance through a PMA approval of this innovative device is granted and patients ... study sites and activities to ensure adherence to appropriate US and OUS regulations , compliance with the study Protocol(s), and applicable local regulations +… more
- Abbott (Sylmar, CA)
- …other regulatory requirements + Aligns with US Food and Drug Administration ( FDA ) regulations , Company policies, operating procedures, processes, and task ... and practices to ensure compliance with federal, state, and local environmental regulations and effective injury and illness prevention programs and well as have… more
- BioLife Plasma Services (Bakersfield, CA)
- …for medical issues. The Medical Support Specialist will be familiar with regulations of the plasma collection industry or a manufacturing environment. The Medical ... to EHS guidance regarding employee incidents. You can be a Pandemic Coordinator when authorized by EHS and support investigations associated with pandemic threats… more
- BioLife Plasma Services (Pomona, CA)
- …for medical issues. The Medical Support Specialist will be familiar with regulations of the plasma collection industry or a manufacturing environment. The Medical ... to EHS guidance regarding employee incidents. You can be a Pandemic Coordinator when authorized by EHS and support investigations associated with pandemic threats… more
- BioLife Plasma Services (Fresno, CA)
- …for medical issues. The Medical Support Specialist will be familiar with regulations of the plasma collection industry or a manufacturing environment. The Medical ... to EHS guidance regarding employee incidents. + You can be a Pandemic Coordinator when authorized by EHS and support investigations associated with pandemic threats… more