| Job alert | Jobs 21 - 30 of 417 |
Clinical Research Associate I - General Internal Medicine
CEDARS-SINAI
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Los Angeles, CA, 90071
... This role follows all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Primary Job Duties and Responsibilities: •Evaluates and abstracts clinical research data from source documents. •Ensures ... - Jun 07
Quality Assurance Inspector
Merle Norman Cosmetics, Inc.
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Los Angeles, CA, 90045
... Essential Duties and Responsibilities · Inspect, test and sample in-process, WIP, final and finished goods according to approved specifications following established work practices, SOPs, FDA and cGMP regulations. Conducts smell analysis, visual ... - Jun 01
Clinical Research Associate I - Cheng Lab, Heart Institute
CEDARS-SINAI
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Los Angeles, CA, 90071
... This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Job Duties and Responsibilities: Works with a Clinical Research Coordinator, Research Program Administrator or ... - Jun 03
Clinical Research Associate I - Gastroenterology and Hepatology
CEDARS-SINAI
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Los Angeles, CA, 90071
... This role follows all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Primary Job Duties and Responsibilities: •Evaluates and abstracts clinical research data from source documents. •Ensures ... - Jun 05
Manufacturing Technician - (FRAC)
Grifols
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Los Angeles, CA
... Strict adherence to procedures and practices according to FDA regulations. Strong emphasis on documentation according to FDA regulations. Adhere to departmental corporate safety policies. Responsible for facility and equipment cleaning. All work is ... - Jun 06
Packaging Associate
BioPhase Solutions
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Los Angeles, CA
... Experience in bottle filling/fine assembly is HIGHLY preferred Proficiency in the English language and communication skills mandatory for following written setup instructions and completing production forms required by FDA and ISO regulations, in ... - May 31
Clinical Research Data Specialist II - Cheng Lab, Heart Institute
CEDARS-SINAI
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Los Angeles, CA, 90071
... Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. Primary Duties and Responsibilities May work with bioinformatics in the development and maintenance of ... - Jun 04
Project Manager
UCLA Health
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Los Angeles, CA, 90009
... and devising solutions, independently organizing and executing regulatory project plans, contributing to quality improvement initiatives and SOP development, and facilitating investigator-initiated trials including FDA submission and reporting. ... - Jun 06
Clinical Research Data Specialist III- Cheng Lab, Heart Institute
CEDARS-SINAI
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Los Angeles, CA, 90071
... Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. Primary Duties and Responsibilities May supervise clinical research staff or clinical data managers. In ... - Jun 04
eCTD Publishing Software Specialist
Insight Global
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Torrance, CA, 90504
... Knowledge of regulatory requirements related to eCTD submissions, including the FDA's Electronic Common Technical Document (eCTD) guidance. null We are a company committed to creating diverse and inclusive environments where people can bring their ... - Jun 04