15 clinical trial coordinator jobs at 8 companies in Temecula, CA
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Clinical Research Coordinator - Hybrid
Irvine, California, United States
$38-$62/hrHybridFull Time
University of California, Irvine: Public research university offering higher education and academic degrees.
3+ YOE3+ years clinical research coordination experience with cancer trials, BA/BS or equivalent, strong communication, problem solving, recordkeeping, and Microsoft Office skills; access to transportation and ability to work outside normal hours.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, OnCore
DermCare Management: Dermatology practice management group providing operational and administrative support.
High school diploma or GED and prior clinical trial experience required; knowledge of medical terminology and regulations, computer proficiency, strong organization, communication, and confidentiality skills required.
Clinical research databases, ECGs, Good Clinical Practice (GCP), Food and Drug Administration (FDA) regulations, HIPAA, OSHA, Standard Operating Procedures (SOPs)
University of California, San Diego: A public research university providing higher education and healthcare.
Bachelor's degree or equivalent experience, clinical trials experience in drug and device research, protocol start-up and regulatory submissions, cardiology research knowledge, data management, and team coordination skills.
Microsoft Office, REDCap, Velos, EPIC, electronic data capture systems, electronic health records, clinical trial management systems
Headlands Research: Operates a multinational network of clinical trial research sites.
2+ YOEMinimum 2 years as primary coordinator on multiple phase 2-4 industry-sponsored trials; bachelor's degree or 2 years college in a health-related program or equivalent experience; strong knowledge of FDA and ICH-GCP; experience with EDC/IVRS and clinical documentation.
Eisenhower Health: Provides comprehensive medical care and hospital services in California.
3+ YOEBachelor's in healthcare (required), 3+ years acute care experience, completion of CITI GCP and CRC courses within 30 days, ACRP CCRC or SOCRA CCRP preferred, proficiency with Microsoft Office, clinical trials and regulatory knowledge.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint
Headlands Research: Operates a multinational network of clinical trial research sites.
2+ YOEMinimum 2 years managing phase 2-4 industry-sponsored clinical trials, knowledge of FDA/ICH-GCP, experience with EDC and IVRS, strong documentation and communication skills, bachelor's or equivalent clinical research training required.
Headlands Research: Operates a multinational network of clinical trial research sites.
2+ YOE2+ years managing phase 2-4 industry-sponsored trials as primary coordinator, HS diploma/GED, knowledge of FDA/ICH-GCP, EDC/IVRS experience, strong documentation and communication skills.
Temporary Clinical Research Regulatory Coordinator
Orange, California, United States
$38/hrHybridFull Time, Temporary
University of California, Irvine: Public research university offering higher education and academic degrees.
Bachelor's degree or equivalent, 3–5 years of clinical research regulatory experience, and knowledge of FDA regulations, GCP, IRB processes, and Phase I–III trials. English proficiency required.
Electronic Medical Records (EMR), OnCore, Complion, Microsoft Excel
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.
Headlands Research: Operates a multinational network of clinical trial research sites.
5+ YOE5+ years as a delegated Clinical Research Coordinator on multiple phase 2-4 trials; proficiency with FDA regulations, CTMS documentation, supervisory experience, and strong communication skills. IATA and GCP required.
NovartisSIX Swiss Exchange, NYSE: NOVN, NVS: A pharmaceutical developing medicines and conducting clinical research.
2+ YOEHigh school diploma and 2+ years in clinical trial or related pharmaceutical logistics required. Requires biological sample shipping knowledge, inventory and documentation skills, and Microsoft Office proficiency.
Microsoft Outlook, Microsoft Word, Microsoft Excel
NovartisNew York Stock Exchange: NVS: Develops and manufactures innovative prescription medicines for patients.
2+ YOEHigh school diploma required; 2+ years in clinical trial logistics or related life sciences industry. Requires biological sample shipping knowledge, inventory and warehouse operations, documentation, and Microsoft Office proficiency.
Microsoft Outlook, Microsoft Word, Microsoft Excel
University of California, Irvine: Public research university offering higher education and academic degrees.
3+ YOE3-5 years related experience with BA/BS or equivalent; strong knowledge of GCP/ICH, clinical trial monitoring/auditing, regulatory compliance, communication, organization, and Microsoft Office proficiency.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint