22 clinical trial coordinator jobs at 11 companies in Pasadena, CA
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Clinical Research Coordinator
Los Angeles, California, United States
$43-$53/hrOnsiteFull Time
The Start: Private early-phase oncology clinical research network serving cancer patients, physicians, and biopharma sponsors.
2+ YOEHigh school diploma or GED and 2 years of clinical research experience required. Requires GCP and regulatory knowledge, oncology trial understanding, accurate documentation, multitasking, and Microsoft Office and clinical trial software proficiency.
Microsoft Office Suite, clinical trial management software
Helios CR, Inc.: U.S. integrated clinical trial network serving patients, physicians, and biopharma sponsors with clinical research services.
3+ YOEBachelor's degree in a health-related field preferred; 3+ years of clinical research experience required. Requires clinical trial coordination, regulatory compliance, participant interaction, data management, and clinical skills.
EMR, Electronic Data Capture (EDC), Study Submission Assistant, EKG
University of California, Irvine: Public land-grant research university and academic health system.
3+ YOE3+ years clinical research coordination experience with cancer trials, BA/BS or equivalent, strong communication, problem solving, recordkeeping, and Microsoft Office skills; access to transportation and ability to work outside normal hours.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, OnCore
First OC Dermatology: Private dermatology practice-management supporting dermatologists and aesthetic-medicine providers across the United States.
High school diploma or GED and prior clinical trial experience required; knowledge of medical terminology and regulations, computer proficiency, strong organization, communication, and confidentiality skills required.
Clinical research databases, ECGs, Good Clinical Practice (GCP), Food and Drug Administration (FDA) regulations, HIPAA, OSHA, Standard Operating Procedures (SOPs)
UCLA Health: Academic medical system providing comprehensive patient care and research.
3+ YOEBachelor's degree or 3–7 years clinical research coordination experience, knowledge of GCP/FDA/ICH regulations, clinical trial budgeting, strong written/oral communication, advanced computer skills, ability to work flexible hours.
Clinical Research Coordinator III, Cardiac Clinical Trials
Los Angeles, California, United States
$71k-$92k/yrOnsiteFull Time
Kaiser Permanente: Integrated managed care consortium and healthcare provider system.
2+ YOEBachelor's in a related field plus 2+ years clinical research experience (or 5+ years without degree). Requires trial documentation, regulatory submissions, compliance knowledge, and BLS preferred.
Artemis Institute for Clinical Research: Multinational clinical trial site network conducting pharmaceutical research for diverse and specialty patient populations.
2+ YOE2+ years coordinating phase 2-4 industry-sponsored trials, knowledge of FDA/ICH-GCP, EDC/IVRS experience, strong documentation, communication, and organizational skills.
Experienced Clinical Research Coordinator - Long Beach
Long Beach, California, United States
$62k-$83k/yrOnsiteFull Time
Healthy Brain Clinic: Private Long Beach medical practice providing memory testing, brain health exams, education, and clinical trials.
2+ YOERequires 2–4+ years coordinating industry-sponsored clinical trials, proficiency with CRIO eSource, CTMS, and EDC platforms, strong attention to detail, and professional spoken and written English.
Clinical Research Coordinator II – Clinical Trials
Los Angeles, California, United States
$29-$49/hrHybridFull Time
Cedars-Sinai: Nonprofit academic medical center providing advanced healthcare and research.
2+ YOEHigh school diploma/GED required; bachelor's degree preferred. Requires 2 years of clinical research experience. SOCRA or ACRP certification preferred.
electronic data capture (EDC) systems, Case Report Forms (CRFs), Institutional Review Board (IRB), Food and Drug Administration (FDA), Good Clinical Practice (GCP), HIPAA
City of Hope: Comprehensive cancer research and treatment organization.
2+ YOECoordinate oncology clinical trials including recruitment, informed consent, protocol execution, data management, and regulatory compliance. Requires bachelor’s degree (or substitute experience), minimum 2 years research/clinical experience, and various certifications within specified timeframes.
University of Southern California: Private research university based in Los Angeles.
0.5+ YOEExperience in clinical trials data management; data entry from medical records; regulatory compliance; sponsor coordination; data quality assurance.