53 clinical research associate jobs at 24 companies in Reseda, CA
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Clinical Research Associate I
Duarte, California, United States
$34-$43/hr OnsiteFull Time
1+ YOEAssociate's degree (or equivalent experience), 1+ year healthcare experience (research preferred), ability to manage protocols, maintain regulatory documents, collect and process specimens, and maintain professional relationships.
2mo
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Clinical Research Associate II
Los Angeles, California, United States
$24-$36/hr OnsiteFull Time
1+ YOEHigh school diploma required; bachelor's in science or sociology preferred. 1+ year clinical research experience. Preferred SOCRA or ACRP certification. Experience with EDCs/CRFs, IRB submissions, GCP and HIPAA compliance, participant scheduling and data collection.
Electronic Data Systems (EDCs)
1mo
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Sr. Clinical Research Associate
Seal Beach, California, United States
$90k-$117k/yr OnsiteFull Time
5+ YOEBachelor's in science or healthcare,5+ years clinical trial experience,3–5 years independent monitoring,GCP/ICH knowledge,SAE reporting,proficiency with EDC/CTMS/EDMS and Microsoft Office,ability to travel up to 75%.
Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Smartsheets
1mo
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Clinical Research Associate (CRA) - Oncology (Remote)
Rahway or New York or Palm Springs or San Diego or Chicago or Orange County or Santa Barbara or Santa Monica or Laguna Hills or Texas or Columbia or Kansas City or St. Louis or Santa Ana or Los Angeles
$96k-$151k/yr RemoteFull Time
2+ YOERequires direct site management experience (≥2 years), clinical research knowledge (ICH/GCP), good documentation and IT skills, valid driver’s license, and ability to travel extensively.
CTMS, eTMF, MS Office
1mo
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Clinical Research Coord, I
Fountain Valley, California, United States
$37-$54/hr OnsiteFull Time
2+ YOEMinimum 2 years clinical research experience, associates required (bachelor's preferred). Must understand protocols, GCP/ICH/FDA regulations, strong data skills, Microsoft Office proficiency, valid driver's license, research/phlebotomy/CITI certifications preferred.
Microsoft Word, Microsoft Excel, Adobe Acrobat
3mo
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Clinical Research Coordinator,RN
Los Angeles, California, United States
$55-$70/hr OnsiteFull Time
2+ YOEAssociate's degree in Nursing; RN license; 2 years clinical research experience; oncology trials knowledge; data accuracy; multitasking; organizational; communication; GCP; MS Office; trial management software.
Microsoft Office, Clinical trial management software
2w
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Clinical Research Associate (CRA) - Oncology (Remote)
New Jersey or New York or Texas or Chicago or Laguna Hills or Los Angeles or Orange County or Palm Springs or San Diego or Santa Ana or Santa Barbara or Santa Monica or Columbia or Kansas City or St. Louis or Rahway or New York City
$96k-$151k/yr RemoteFull Time
2+ YOEAssociate degree or certificate in a scientific or healthcare discipline plus 5 years' experience, including 2 years of site monitoring, or bachelor's degree plus 2 years of direct site management in bio/pharma or CRO.
CTMS, eTMF, Microsoft Office, Microsoft Excel
3w
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Senior Clinical Research Associate, Field Monitor
El Segundo or Los Angeles or San Diego or San Francisco or New York City or Chicago or Boston
$128k-$136k/yr RemoteFull Time
6+ YOEBachelor's degree (or RN with 5+ years monitoring),6+ years clinical trial experience,4+ years on-site/remote monitoring,valid driver's license,knowledge of ICH‑GCP,EDC/eTMF/CTMS and MS Office,ability to travel 50–75%.
EDC, eTMF, CTMS, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Adobe
1mo
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Clinical Research Coord II, Oncology
Orange, California, United States
$31-$51/hr OnsiteFull Time
3+ YOEMinimum 3 years clinical research coordination; associate degree or equivalent experience; BLS required; knowledge of ICH-GCP, human subjects regulations, Microsoft Office; Cerner experience preferred.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Cerner
1w
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Clinical Research Data Specialist I
Los Angeles, California, United States
$27-$31/hr OnsiteFull Time
0.5+ YOEAssociate's degree or equivalent experience, 1 year clinical trial experience, attention to detail, data entry, medical terminology, and compliance with clinical research standards.
REDCap, Microsoft Access, SQL Server, Electronic Medical Records (EMR)
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Research Associate
Santa Ana, California, United States
$29-$36/hr OnsiteFull Time
2+ YOEBachelor's in public health or related field, 2+ years handling infectious agents in clinical/public health lab, research experience, phlebotomy preferred, valid CA driver license, TB testing and N-95 fit testing required.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft SharePoint, Microsoft OneDrive, REDCap, Cerner, Electronic Test Orders and Results (ETOR)
3mo
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Senior Clinical Research Associate - Remote Position
Los Angeles, California, United States
$140k-$165k/yr RemoteFull Time
5+ YOEBachelor's degree; 5+ years health-related experience, including 3+ years CRA; strong ICH GCP/FDA knowledge; oncology/global trials preferred.
Electronic Data Capture (EDC), Word Processing, Spreadsheet, Document Management Systems
2mo
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Assistant Clinical Research Coordinator
Inglewood, California, United States
$20-$26/hr OnsiteFull Time
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
1w
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Clinical Research Data Specialist I
Los Angeles, California, United States
$27-$31/hr OnsiteFull Time
1+ YOERequires 1 year of clinical trial experience, attention to detail, regulatory compliance knowledge, and data entry experience. Associate's degree required; medical terminology knowledge preferred.
REDCap, Microsoft Access, SQL Server, Electronic Medical Records (EMR)
1mo
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Senior Clinical Trials Management Associate
Santa Monica or Foster City or El Segundo or Parsippany
$115k-$164k/yr OnsiteFull Time
2+ YOEExperience in clinical research operations, interpretation of FDA/ICH guidelines, study start-up, document generation/review, vendor management, and metrics reporting. BS/BA +4yrs OR MS/MA +2yrs required; oncology clinical trial experience preferred.
Workday
2w
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Clinical Contracts Associate II
Plano or Maple Grove or Santa Clara or Sylmar
$61k-$123k/yr OnsiteFull Time
5+ YOEDeveloping and negotiating clinical study contracts and complex budgets; 5+ years clinical research experience, strong written and verbal communication, GCP knowledge, and ability to travel domestically as needed.
Microsoft Excel, Power BI
1mo
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Scientific Content & Clinical Associate
Carson, California, United States
$30/hr OnsiteFull Time
Currently pursuing or recently completed degree in life sciences/chemistry/related field; strong research, technical writing, and analytical skills; proficiency in Microsoft Office; familiarity with scientific literature.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
2w
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Clinical Contracts Associate II
Plano or Maple Grove or Santa Clara or Sylmar
$61k-$123k/yr OnsiteFull Time
5+ YOEBachelor's degree or equivalent experience, 5+ years clinical research/contracts experience, GCP knowledge, strong communication, negotiation and budget skills, domestic travel as needed.
Microsoft Excel, Power BI
1mo
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Associate Director, Clinical Pharmacology
Thousand Oaks or San Francisco
$205k-$235k/yr OnsiteFull Time
8+ YOEPharmD or PhD preferred; 8+ years clinical pharmacology experience with small molecules; Phase 1 study design experience; proficiency with Phoenix WinNonLin; regulatory submission experience; strong communication and independent working skills.
Phoenix WinNonLin
2mo
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Clinical Scientist Associate Director, Late Development Oncology
United States or Thousand Oaks
$170k-$230k/yr RemoteFull Time
3+ YOEDegree-based clinical development experience required (Doctorate+3yr, Master’s+5yr, Bachelor’s+7yr, Associate+12yr, HS+14yr). Experience with clinical trial protocol development, data review, GCP compliance, and clinical data analysis; oncology preferred.
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