118 research coordinator jobs at 56 companies in Acton, CA
4d
Save
Mark Applied
Hide
4d
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 2+ years clinical research coordination experience, proficiency with Adobe and Microsoft Excel, knowledge of clinical research regulations, strong communication and organizational skills.
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.
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.
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 required; 1+ years clinical research experience preferred. Phlebotomy or MA certification preferred. Knowledge of GCP, informed consent, specimen handling, and electronic data capture required.
REDCap, Electronic Data Capture (EDC), Microsoft Office
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.
Providence: A non-profit health system providing comprehensive medical care services.
2+ YOECompletion of medical or phlebotomy training or equivalent experience; 2 years of clinical research experience required, 3 preferred. College degree, phlebotomy certificate, biohazardous materials training, and bilingual English/Spanish skills may be required or preferred.
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
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)
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
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.
CAIR California: Protects civil rights and provides legal services for Muslims.
2+ YOE2+ years experience monitoring social media or related research; strong written communication, attention to detail, familiarity with major social platforms, spreadsheet skills, ability to travel to events, and interest in civil rights/advocacy.
X/Twitter, Instagram, Facebook, TikTok, Canva, Google Slides, CapCut
RadNetNASDAQ: RDNT: Provider of outpatient diagnostic imaging and radiology services.
Coordinate patient visits, manage study correspondence and scheduling, maintain tracking records; high school diploma required, 1+ year medical/research experience preferred, strong organizational and communication skills.