141 research coordinator jobs at 73 companies in Stanton, CA
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Clinical Research Coordinator
Los Angeles, California, United States
$38-$61/hrHybridFull Time
UCLA Health: Provides comprehensive hospital services and academic medical research.
1+ YOEBachelor's degree or 1+ years clinical research coordination experience; strong communication, organizational, analytical, computer and budgeting skills; working knowledge of FDA CFR and ICH GCP; flexible hours and travel.
University of Southern California: Private research university providing higher education and healthcare services.
1+ YOEBachelor's degree or equivalent,1+ year administrative or research experience,MS Office proficiency,excellent communication,attention to detail,ability to manage recruitment, data collection, and regulatory compliance.
Loma Linda University Health: Nonprofit academic medical center providing healthcare and higher education.
1+ YOEHigh school diploma/GED, 1+ year healthcare or clinical research experience, EMR proficiency, IATA certificate within 90 days, Certified Clinical Research Coordinator within eligibility, strong communication and attention to detail.
Cedars-Sinai: Provides academic medical care, specialized treatment, and biomedical 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.
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.
New York University: A private research university providing higher education degree programs.
Master's degree or higher in social work, public health, psychology, nursing or related field; research and participant-tracking experience; strong organization, attention to detail, and ability to travel within Los Angeles; authorized to work in the US.
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
Alliance Clinical Network: Operates medical research sites for Phase I-IV clinical trials.
Support coordination and execution of clinical research studies, participant screening, consent, data collection, specimen handling, and regulatory compliance; knowledge of GCP/HIPAA preferred.
Electronic data capture systems, Clinical trial management software, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
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
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)
University of California, Irvine: Public research university offering higher education and academic degrees.
2+ YOE2+ years CRC experience, knowledge of clinical research processes and GCP, strong data management, ability to follow complex protocols, English proficiency.
Chapman University: A private university offering undergraduate and graduate degree programs.
2+ YOE2+ years clinical or administrative experience, strong organization, communication, ability to work independently, flexibility for evenings/weekends, experience with human subjects and data collection preferred.
CenExel: Operates a nationwide network of clinical research sites.
1+ YOE1+ year CRC experience required, knowledge of ICH/GCP and federal human subjects regulations, high school diploma (bachelor's preferred), strong communication, leadership, and problem-solving skills.
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.
Claremont McKenna College: Private liberal arts college providing undergraduate education and research.
Supports faculty pre-award activities: coordinating proposal documents and portals, tracking opportunities and deadlines, assisting budget development, and translating technical grant language for stakeholders.
Grants.gov, ProposalCentral, Research.gov, eRA Commons