87 clinical research coordinator jobs at 28 companies in El Monte, CA
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Clinical Research Coordinator
Beverly Hills or Los Angeles
$32-$34/hrFieldFull Time
Beverly Hills Cancer Center: Private academic cancer center providing comprehensive oncology treatment, imaging, research, and clinical trials for Southern California patients.
2+ YOERequires 2+ years of clinical research coordinator experience, 1+ year of oncology research experience, and a bachelor's degree; related science, healthcare, or nursing field preferred. CCRP preferred.
UCLA Health: Academic medical system providing comprehensive patient care and research.
2+ YOEBachelor's degree or 2+ years clinical research coordination experience, proficiency with Adobe and Microsoft Excel, knowledge of clinical research regulations, strong communication and organizational skills.
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
Providence Medical Foundation: Catholic nonprofit medical foundation providing primary and specialty care to California patients through physician groups and networks.
2+ YOEMedical or phlebotomy training required; clinical research experience required, with 2 years minimum and 3 preferred. College degree and phlebotomy certificate may be required by department.
Providence Medical Foundation: Catholic nonprofit medical foundation providing primary and specialty care to California patients through physician groups and networks.
2+ YOECompletion of accredited medical or phlebotomy training or equivalent; 2 years clinical research experience required, 3 preferred. Phlebotomy certificate may be required; bilingual English/Spanish preferred.
Institutional Review Board (IRB), Good Clinical Practice (GCP), International Council for Harmonisation (ICH)
University of California, Irvine: Public land-grant research university and academic health system.
3+ YOERequires 3–5 years as a clinical research coordinator, clinical research and human-subject regulations knowledge, data management, protocol and GCP compliance skills, communication, organization, and English proficiency.
Electronic Data Capture (EDC), clinical research databases, case report forms (CRFs), Good Clinical Practice (GCP), standard operating procedures (SOPs)
Elite Clinical Network: Private clinical research site network serving pharmaceutical companies, CROs, physicians, and study participants in Phase I–IV trials.
1+ YOEBachelor's in health-related field required; 1+ year clinical research experience preferred; phlebotomy or MA certification preferred; GCP knowledge; Microsoft Office and REDCap proficiency; strong organization and communication.
Velocity Clinical Research: Clinical research site organization conducting Phase I–IV trials for pharma and biotech companies across U.S. and Europe.
2+ YOERequires a bachelor's degree plus 2 years, associate's plus 4 years, or high school/technical degree plus 6 years of life science experience, including 1 year coordinating clinical research; English proficiency required.
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
Cedars-Sinai: Nonprofit academic medical center providing advanced healthcare and research.
5+ YOEBachelor's degree required (Master's preferred). SoCRA or ACRP within 1 year, BLS required, CPT and CRMA preferred. Minimum 5 years clinical research coordination experience and experience leading/coordinating staff.
National Institute of Clinical Research: Physician-owned U.S. clinical-trial management organization conducting multi-site studies for pharmaceutical and biotechnology sponsors.
2+ YOEBachelor’s degree preferred; 2-3 years clinical research coordination; local to Orange County; GCP, FDA, IRB knowledge; CCR or CCRP preferred.
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)
Children's Hospital of Orange County: Nonprofit pediatric healthcare system providing hospital, specialty care and research for children in Southern California.
1+ YOEMinimum 1 year clinical research coordination experience; associate degree or equivalent experience; RQI Responder (AHA) required within 6 months; phlebotomy preferred; working knowledge of ICH-GCP; proficiency with Microsoft Office and strong communication skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Cerner
PIH Health Hospital - Whittier: A nonprofit regional healthcare network providing integrated hospital and healthcare services.
2+ YOERequires high school diploma/GED, 2–3 years in a hospital or academic medical center, 2–3 years in clinical research, medical terminology knowledge, and current human subjects protection and Good Clinical Practice training.
Salma Health: Private brain health providing integrated mental, neurological, and neuropsychiatric care, diagnostics, research, and technology to patients.
3+ YOEBachelor’s degree in a health or life science field, 3+ years of clinical research experience, regulatory submission expertise, FDA/GCP knowledge, and phlebotomy ability or certification willingness.
REDCap, Medidata Rave, electronic data capture (EDC), CITI Program
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.
Alliance Clinical Network: Private clinical research site network serving patients, pharmaceutical sponsors, and contract research organizations through diverse clinical trials.
High school diploma required (associate preferred); basic clinical research knowledge; MA or phlebotomy and CPR/BLS preferred; experience in research/healthcare, GCP/HIPAA knowledge, and proficiency with electronic data capture, CTMS, and Microsoft Office preferred.
electronic data capture systems, clinical trial management software, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
Loma Linda University Health: Academic medical center and faith-based health sciences institution.
4+ YOEBachelors in related field and minimum 4 years clinical research experience. BLS required, IATA within 90 days; MA/CNA/phlebotomy preferred. Knowledge of HIPAA, FDA/ICH, data management, and strong communication skills.