53 clinical research coordinator entry level jobs at 21 companies in Pasadena, CA
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Clinical Research Coordinator - Clinical Research
Sherman Oaks, California, United States
$29-$34/hrOnsiteFull Time
CenExel: Operates a nationwide network of clinical research sites.
1+ YOEHigh school diploma or equivalent and 1+ year of clinical research coordinator experience required; bachelor's degree preferred. Requires clinical trial regulations knowledge, communication, problem-solving, and teamwork skills.
UCLA Health: Provides comprehensive hospital services and academic medical research.
2+ YOEBachelor's degree (or equivalent), 2+ years clinical research/study coordination experience, strong communication and analytical skills, attention to detail, proficiency with Adobe and Microsoft Excel, and availability to travel to clinic sites.
Cedars-Sinai: Provides academic medical care, specialized treatment, and biomedical research.
1+ YOECoordinate clinical studies, screen and consent patients, maintain source documents and CRFs, ensure timely data entry and regulatory compliance; 1+ year clinical research experience, HS diploma minimum, bachelor\u0002s preferred.
The START Center for Cancer Research: Global network of early-phase oncology clinical trial sites.
2+ YOEHigh School diploma/GED, 2 years clinical research experience, working knowledge of GCP and regulatory requirements, Phase 1 oncology familiarity preferred, strong communication and organizational skills, proficiency with Microsoft Office and clinical trial management software.
Microsoft Office Suite, clinical trial management software
Providence: Provides comprehensive healthcare services through hospitals, clinics, and health plans.
2+ YOEMedical or phlebotomy training required; college degree, phlebotomy certificate, biohazardous-material packaging training, English/Spanish skills, and 2 years of clinical research experience preferred.
Providence: Non-profit health system providing comprehensive medical and social services.
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)
Elite Clinical Network: Clinical research network operating sites for pharmaceutical trials.
1+ YOEBachelor's in a health-related field, 1–2 years clinical research experience preferred, phlebotomy or MA certification preferred, GCP knowledge, REDCap and Microsoft Office proficiency, strong organization and communication.
Helios Clinical Research: Integrated clinical trial site network for medical research
2+ YOEBachelor's preferred, 2 years clinical research experience, regulatory and study coordination skills, phlebotomy, vital signs and ECG competence, participant recruitment and informed consent.
CHOC: Provides specialized medical care and healthcare services for children.
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
Clinical Research Coordinator III, Cardiac Clinical Trials
Los Angeles, California, United States
$71k-$92k/yrOnsiteFull Time
Kaiser Permanente: Provides integrated medical care and health insurance plans.
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.
Beverly Hills Cancer Center: Provides comprehensive cancer treatment and diagnostic imaging services.
2+ YOE2+ years CRC experience (1+ year oncology), bachelor\u0002s degree required, CCRP preferred, experience with EMR/CTMS/eCRF, strong communication and organizational skills.
Alliance Clinical Network: Operates medical research sites for Phase I-IV 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
Clinical Research Coordinator I - Westside Los Angeles
Los Angeles, California, United States
$27/hrOnsiteFull Time
Irvine Clinical Research: Conducts clinical trials specializing in neurology and psychiatry.
Coordinate clinical trial operations, perform study procedures per GCP/protocols, maintain study data, recruit and screen participants; bachelor's/masters/nursing degree required; strong attention to detail and English proficiency.
University of Southern California: Private research university providing higher education and healthcare services.
2+ YOEBachelor's degree and 2+ years clinical research or phlebotomy experience; must hold a California phlebotomy license; knowledge of GCP/HIPAA; MS Office proficiency and strong communication skills.
Medical Assistant/JR Clinical Research Coordinator
Huntington Beach, California, United States
$18-$32/hrOnsiteFull Time
National Institute of Clinical Research: A research organization running clinical trial sites and supporting pharmaceutical and biotech studies.
2+ YOEMedical assistant or phlebotomist with 2+ years clinical experience, phlebotomy skills, EMR/word processing ability, bilingual English/Spanish preferred, and ability to perform EKGs, vitals, and specimen collection.
Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)
Arcadia, California, United States
$34-$56/hrOnsiteFull Time
Keck Medicine of USC: Provides specialized medical care and research via university health system.
2+ YOECoordinates study recruitment, scheduling, data collection, regulatory documentation, and participant education; requires bachelor's or equivalent experience, 2 years research/administrative experience, MS Office proficiency, and CITI/GCP/HIPAA training.
Microsoft Office, Electronic Medical Records (EMR)