38 clinical data coordinator jobs at 26 companies in Stanton, CA
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Clinical Research Coordinator III, Clinical Trials, Vaccine Research (Durational with Benefits)
Ontario, California, United States
$71k-$92k/yrOnsiteFull Time
Kaiser Permanente: Provides integrated medical care and health insurance plans.
2+ YOECollects and documents clinical trial data, prepares regulatory submissions, ensures compliance, and supports protocol implementation; requires clinical research experience and ability to interact with stakeholders.
The START Center for Cancer Research: Global network of early-phase oncology clinical trial sites.
2+ YOEHigh school diploma/GED, 2 years clinical data entry experience, computer/office skills, CRF/clinical data management, familiarity with medical terminology; CCRP or CCRC and bachelor’s preferred.
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
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.
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
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.
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.
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.
Prime Healthcare Services: Operates a nationwide network of acute care hospitals.
Bachelor's degree in computer science or related field, experience with EHR systems, knowledge of Medi‑Cal/third‑party billing and billing regulations, and ability to prepare billing reports and coordinate EDI submissions.
Electronic Health Record (HER), Electronic data interface (EDI)
Loma Linda University Health: Nonprofit academic medical center providing healthcare and higher education.
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.
Prime Healthcare: Operates community hospitals and provides healthcare services.
Bachelor's degree in computer science or related field, experience with EHR systems, knowledge of Medi‑Cal/third‑party billing and billing regulations, and ability to prepare and analyze billing reports.
Electronic Health Record (HER), Electronic Data Interchange (EDI)
WelbeHealth: Provides all-inclusive medical and social care for elderly seniors.
2+ YOEUnencumbered RN license, graduate of an accredited nursing program, 2+ years clinical nursing with frail/elderly population, supervisory and care coordination experience preferred, data-driven leadership, willing to work varied schedule including nights/weekends/overtime.
CHA Hollywood Presbyterian Medical Center: Acute care hospital providing comprehensive medical and surgical services.
Coordinate clinical quality measures, perform clinical/regulatory review, abstract and analyze outcome data, design dashboards and reports, and support medical staff quality review. Clinical license often required.
Lorian Health: Provides personalized home health and hospice care services.
Coordinating intake/referrals, maintaining clinical field staff schedules, entering patient data into EMR/HCHB, strong Microsoft Office and phone skills, medical terminology knowledge, HIPAA compliance.
Microsoft Word, Microsoft Excel, HomeCare HomeBase (HCHB), EMR
AHMC Healthcare: Operates a network of acute care hospitals and medical centers.
2+ YOECoordinate medical staff peer review, abstract and validate clinical data, support performance improvement and regulatory compliance; 2+ years quality/risk/case management experience preferred; clinical degree and CA RN/LVN preferred; Microsoft Office, Google Workspace, MicroMed skills.
Green Meadows Home Health: Provides skilled nursing and therapy services at home.
1+ YOEManage intake from referral through admission, verify eligibility and insurance, enter data into EMR, coordinate with clinical staff, and ensure compliance with Medicare/Medicaid/HIPAA. Requires 1+ year healthcare or intake experience preferred and strong communication/organizational skills.
Sr. Clinical Trials Associate - Onsite in Aliso Viejo, CA
Aliso Viejo, California, United States
$108k-$135k/yrOnsiteFull Time
GlaukosNYSE: GKOS: Develops therapies and devices for treating chronic eye diseases.
5+ YOE5-8 years CTA experience in ophthalmic field, bachelor's in science preferred, ability to coordinate clinical trials, review and clean data, maintain study master file, support audits, and lead meetings.