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Job alert Jobs 31 - 40 of 334

Sr. QC Analyst

BioPhase Solutions  –  Los Angeles, CA
... Plate Readers, Flow Cytometry, PCR, and HPLC Knowledge of cGMP, FDA, and USP regulations and a basic understanding of statistics Knowledge of MS Word and Excel Please send resumes to and visit our website at for additional job opportunities! - Apr 26

Clinical Research Coordinator

UCLA Health  –  Los Angeles, CA
... You will be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical ... - May 06

Clinical Research Associate I - Department of Neurology (Hybrid)

CEDARS-SINAI  –  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: Completes Case Report Forms (CRFs). Enters clinical research data into Electronic ... - May 06

Clinical Research Associate I - Nuclear Medicine

CEDARS-SINAI  –  Beverly Hills, CA, 90213
... 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 ... - May 07

Clinical Research Associate I - Regenerative Medicine Institute

CEDARS-SINAI  –  Los Angeles, CA, 90071
... Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations about the study and patient care. Primary Duties & Responsibilities: Works with a Clinical Research Coordinator, Research Program Administrator, or Research ... - May 07

Clinical Research Associate I - Nuclear Medicine

CEDARS-SINAI  –  Beverly Hills, CA, 90213
... 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 ... - May 06

Clinical Research Coordinator, Torrance

UCLA Health  –  Torrance, CA
... You will be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical ... - Apr 29

Food Quality Control Technician

TalentZok  –  Los Angeles, CA
... Immediate opening for a Food Quality Control Technician in San Pedro, CA who possesses: Quality and/or Food Production/Processing Experience (FDA/USDC) - 1+ yrs. MS Office/Excel/Word/Outlook Bilingual Spanish HS Diploma or GED Required Email resumes ... - May 03

Contracts Manager (REMOTE)

Platinum Resource Group  –  Los Angeles, CA
... Strong understanding of clinical trial regulations and guidelines (e.g., ICH-GCP, FDA regulations). Excellent negotiation, communication, and interpersonal skills. Ability to prioritize tasks, manage multiple projects simultaneously, and meet ... - May 01

Clinical Research Associate I - Regenerative Medicine Institute

CEDARS-SINAI  –  Los Angeles, CA, 90071
... Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations about the study and patient care. Primary Duties & Responsibilities: Works with a Clinical Research Coordinator, Research Program Administrator, or Research ... - May 06
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