14 clinical research coordinator jobs at 9 companies in Nevada
2mo
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Clinical Research Coordinator
Sugar Land or Alabama or Arizona or Florida or Georgia or Illinois or Massachusetts or Michigan or Missouri or Nevada or South Carolina or Texas or Virginia or Puerto Rico
OnsiteFull Time
1+ YOEMinimum 1 year clinical or clinical research experience and a Medical Assistant diploma, LPN/LVN, EMT, or Associate's degree; proficiency with basic clinical procedures (vitals, EKGs, phlebotomy), EDC/EHR and Microsoft apps; strong communication and organizational skills.
Microsoft applications, email, electronic health records, web applications, EDC
2mo
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Travel Clinical Research Coordinator - Nevada
North Las Vegas, Nevada, United States
FieldFull Time
3+ YOEBachelor’s degree in health, life sciences, nursing, or related field; 3–4 years of clinical research coordinator experience; strong GCP, GDP, ALCOA+, EDC, CTMS, regulatory, and multi-site operations knowledge.
Medidata Rave, Veeva, Oracle, CTMS, EDC
5d
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Clinical Research Coordinator
Katy or Alabama or Arizona or Florida or Georgia or Illinois or Massachusetts or Michigan or Missouri or Nevada or Virginia or South Carolina or Tennessee or Texas or Puerto Rico
OnsiteFull Time
1+ YOERequires a medical assistant diploma, LPN/LVN, EMT credential, or associate's degree plus 1 year of clinical research or clinical experience; basic clinical procedures and computer proficiency required.
Microsoft applications, Electronic Health Records, email, web applications, ECG, EDC
6d
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Clinical Research Coordinator
Maitland or Alabama or Arizona or Florida or Georgia or Illinois or Massachusetts or Michigan or Missouri or Nevada or Virginia or South Carolina or Tennessee or Texas or Puerto Rico
OnsiteFull Time
1+ YOEMedical Assistant diploma, LPN/LVN, EMT credential, or associate degree plus 1 year clinical research or clinical experience; clinical procedures, computer applications, communication, organization, and confidentiality skills required.
Microsoft applications, email, electronic health records, web applications
1mo
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Travel Clinical Research Coordinator
Lake Mary or Alabama or Arizona or Florida or Georgia or Illinois or Massachusetts or Michigan or Missouri or Nevada or Virginia or South Carolina or Tennessee or Texas or Puerto Rico
FieldFull Time
2+ YOE2+ years clinical research coordination experience, MA/LPN/LVN/EMT credential, vaccine trial experience required, proficiency with basic clinical procedures, EDC and Microsoft applications.
Microsoft, EDC
2mo
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Clinical Research Coordinator
Las Vegas, Nevada, United States
OnsiteFull Time
4+ YOEBachelor's in a health field, 4+ years CRC experience, phlebotomy certification and experience, knowledge of GCP and regulatory guidelines, proficiency with Microsoft Office and EDC/REDCap.
Microsoft Office, REDCap, EDC
3w
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Clinical Research Coordinator (51879)
San Diego or Texas or Arizona or California or Nevada or Florida
$28-$31/hr FieldFull Time
Bachelor's degree required; three years of experience, phlebotomy knowledge, research regulatory knowledge, computer skills, communication skills, and a valid driver's license required. CCRC preferred.
Case Report Form (CRF), fax, copier, printer, telephone, calculator
3mo
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Clinical Research Coordinator II (Relocation Opportunity)
Dalton or California or Louisiana or Washington or Nevada
$60k-$90k/yr OnsiteFull Time
3+ YOE3+ years CRC experience, recent phlebotomy experience, GCP and federal regs knowledge, ability to perform basic clinical procedures, strong documentation and EDC/IVR skills, leadership and communication abilities.
clinical trials database, IVR systems, IVRS, electronic data capture, EDC, MS Word, Microsoft Excel
1mo
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Clinical Research Coordinator
Henderson, Nevada, United States
OnsiteFull Time
3+ YOEBachelor's in a health-related field, 3 years CRC experience, phlebotomy certification, GCP knowledge, Microsoft Office and REDCap/EDC proficiency, strong communication and organizational skills.
Microsoft Office, REDCap, EDC platforms
2mo
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PS Clinical Research Coord
Salt Lake City or Idaho or Montana or Nevada or Utah or Wyoming
$61k/yr OnsiteFull Time
2+ YOEBachelor's in health sciences or equivalent with 2 years professional research experience; completion of University RATS Clinical Certification within one year of hire; knowledge of GCP, FDA, HIPAA, IRB regulations; strong organization and communication skills.
1mo
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Clinical Trials Regulatory Coordinator, Research Department, Kirk Kerkorian School of Medicine[R0152658]
Las Vegas, Nevada, United States
OnsiteFull Time
2+ YOEBachelor's degree and minimum 2 years clinical regulatory research experience; knowledge of IRB, GCP, FDA regulations; experience with clinical trial document preparation and maintenance.
2mo
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Research Nurse
Norfolk or Alabama or Delaware or Florida or Georgia or Idaho or Indiana or Kansas or Louisiana or Maine or Maryland or Minnesota or Nebraska or Nevada or New Hampshire or North Carolina or North Dakota or Ohio or Oklahoma or Pennsylvania or South Carolina or South Dakota or Tennessee or Texas or Utah or Virginia or Washington or West Virginia or Wisconsin or Wyoming
OnsiteFull Time
2+ YOEBSN required; active Virginia RN license or compact/multi-state eligible; BLS within 90 days; specialty research certification (CCRP/ACRP-CP or CCRC) required within 3 years; minimum 2 years experience; clinical research coordination skills.
5d
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Monitoring Excellence Academy - Oncology / CART/ Ophthalmology - CRA 1 - Central or West
United States or South Dakota or Michigan or Ohio or Illinois or California or Oklahoma or Utah or Missouri or Arizona or Idaho or Tennessee or Nevada or Washington or Oregon or Wisconsin or Montana or Texas or Colorado or Montreal or New Mexico or Indiana or Kansas or North Dakota or Durham
$80k-$90k/yr RemoteFull Time
University or college degree or allied health certification, 2+ years as a study coordinator or research nurse, and oncology, ophthalmology, or CAR T experience. Requires 60–70% overnight travel.
Case Report Forms (CRFs)
2d
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Data Compliance Coordinator
Las Vegas, Nevada, United States
OnsiteFull Time
Preferred clinical research or data management experience; knowledge of ICH/GCP, regulatory and data protection requirements; eCRF entry, query resolution, ISF documentation, Microsoft Office, and English communication skills.
Electronic Case Report Form (eCRF), Microsoft Office