18 clinical study coordinator jobs at 10 companies in Los Angeles, CA
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Clinical Study Coord
Irvine, California, United States
$45-$70/hrOnsiteFull Time
City of Hope: Medical research and treatment center for cancer and diabetes.
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.
UCLA Health: Provides comprehensive hospital services and academic medical research.
1+ YOEBachelor's degree or 1–3 years of study or clinical research coordination experience; strong communication, organization, analytical, computer, regulatory, budgeting, and clinical research skills required.
Duarte or Los Angeles or Orange County or Atlanta or Chicago or Phoenix
OnsiteFull Time
City of Hope: Medical research and treatment center for cancer and diabetes.
2+ YOEBachelor's in science/health preferred (substitutable by additional experience). Minimum 2 years research or clinical experience. Must obtain ACRP or SOCRA within 1 year; IATA, GCP, HSP, and BLS within 1 month. Understand/apply FDA, OHRP, GCP/ICH, HIPAA; execute protocols; coordinate recruitment/consent; monitor participants and report adverse even...
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.
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.
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.
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.
Clinical Research Coordinator - Neurology (limited, part-time)
Los Angeles, California, United States
$38-$61/hrHybridPart Time, Temporary
UCLA Health: Provides comprehensive hospital services and academic medical research.
1+ YOEBachelor's degree or 1–3 years of study coordination experience; strong communication, organization, analytical, computer, regulatory, budgeting, and interpersonal skills required.
Helios Clinical Research: Integrated clinical trial site network for medical research
6+ YOEOversee CRCs and RAs for oncology trials; ensure ICH-GCP/FDA/HIPAA compliance; manage study start-up, regulatory submissions, data quality, and budgets. Bachelor's preferred; CCRC and phlebotomy desired; 6+ years clinical research experience.
University of Southern California: Private research university providing higher education and clinical services.
Provide high-quality urologic patient care, develop management plans, coordinate referrals, document encounters, perform/interpret diagnostic studies, assist with procedures, and participate in clinical education.
Clinical Research Associate I - Heart Institute - Bairey-Merz Lab
Los Angeles, California, United States
$25-$34/hrOnsiteFull Time
Cedars-Sinai: Provides academic medical care, specialized treatment, and biomedical research.
1+ YOEAssist coordination of noncomplex clinical studies, collect and abstract research data, complete CRFs, enter data into sponsor EDCs, assist with IRB submissions and study logistics; HS diploma required, Bachelors preferred.
Clinical Research Program Manager - Quality Outcome & Grant Writing
Irvine, California, United States
$90k-$120k/yrOnsiteFull Time
Pacific Neuropsychiatric Specialists: Provides outpatient psychiatric and mental health care services.
2+ YOEMaster's degree required, 2+ years clinical research or study coordination experience, IRB experience, strong scientific and grant writing, project management, Microsoft Office and reference manager proficiency.
Microsoft Office, EndNote, Zotero, Mendeley, REDCap
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)
CenExel: Operates a nationwide network of clinical research sites.
High school diploma or GED, excellent interpersonal skills, self-motivation, ability to work independently, professional presentation, and completion of study coordinator training requirements.
Los Angeles or Santa Monica or Westwood or Marina del Rey or Culver City
$38-$61/hrFieldFull Time, Temporary
UCLA Health: Provides comprehensive hospital services and academic medical research.
2+ YOEBachelor's degree or 2+ years of study coordination experience; clinical research, regulatory, patient communication, organizational, analytical, Adobe, Microsoft Suite, and Excel skills required.
AIDS Healthcare Foundation: Global nonprofit providing HIV/AIDS medical care and advocacy services.
Leads daily public health research operations, oversees research staff, coordinates study implementation, partners with stakeholders, improves clinic workflows, conducts literature reviews, and supports manuscript writing.