23 clinical research coordinator entry level jobs at 14 companies in Mesa, AZ
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Clinical Research Coordinator Oncology
Gilbert, Arizona, United States
OnsiteFull Time
2+ YOECoordinate clinical trial protocols, collect and record medical data, assist patient assessments, maintain study files; requires bachelor's in healthcare, 2+ years clinical research experience, CRCC preferred.
1w
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Clinical Research Coordinator
Peoria, Arizona, United States
OnsiteFull Time
2+ YOERequires 2–3 years of clinical research experience, English communication, medical terminology, Microsoft Office proficiency, and a valid driver's license; associate or bachelor's degree preferred.
Redcap, Medidata Rave, Microsoft Office Suite, Microsoft Word, Microsoft Excel, Microsoft Outlook, Clinical Trial Management Systems (CTMS)
4w
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Clinical Research Coordinator
Sun City, Arizona, United States
OnsiteFull Time
1+ YOEBachelor's in health-related field required; 1+ years clinical research experience preferred; phlebotomy or MA certification preferred; GCP knowledge; proficiency with Microsoft Office and REDCap.
Microsoft Office, REDCap
3mo
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Clinical Research Coordinator I - Nurse
Sun City, Arizona, United States
OnsiteFull Time
1+ YOERN license required; 1-3 years clinical research coordinating experience preferred.
Clinical Trial Management System (CTMS)
1w
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Clinical Research Coordinator
Phoenix, Arizona, United States
$46k-$68k/yr OnsiteFull Time
1+ YOEBachelor’s degree in biological sciences or related medical/scientific field, 1–2 years of related healthcare or clinical research experience, BLS, Arizona driver’s license, human subjects protection training, and English proficiency.
Microsoft Office
2w
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Coordinator II - Clinical Research- Oncology
Scottsdale, Arizona, United States
OnsiteFull Time
2+ YOE2+ years clinical/research or data management experience, BLS required, clinical research certification preferred, knowledge of ICH/GCP and FDA regulations, strong writing and computer skills.
Microsoft Word, Microsoft Excel, Microsoft Access, EDC
1mo
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Clinical Research Coordinator I
Phoenix, Arizona, United States
$55k-$65k/yr OnsiteFull Time
Supports clinical trials from startup through closeout; follows GCP/ALCOA-C/IATA/HIPAA standards; preferred 1 year research and 1 year direct patient experience; proficiency with Microsoft Office and EDC.
EDC, Microsoft Excel, Microsoft Word, Microsoft Outlook
2mo
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Clinical Research Coordinator I
Phoenix, Arizona, United States
OnsiteFull Time
1+ YOECoordinate clinical research at investigative sites, ensure protocol and regulatory compliance, train staff, and manage data entry and documentation.
EDC, IVRS, Laboratory Information Systems
1mo
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Clinical Research Coordinator I - Strong Heart Study - Phoenix, Arizona
Phoenix, Arizona, United States
$49k-$87k/yr OnsiteFull Time
1+ YOEHS/GED required; 1-2 years clinical research experience; IRB and regulatory support, CTMS data entry, biospecimen handling, IATA and OSHA training; bachelor's preferred.
Clinical Trial Management System (CTMS)
1mo
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Clinical Research Coordinator I (3932)
Phoenix, Arizona, United States
OnsiteFull Time
1+ YOEComplete required GCP/IATA training, conduct study visits, document data per ALCOA-C, resolve queries, and support participant recruitment and consent.
EDC, IVRS
1mo
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Clinical Research Coordinator I (103304)
Phoenix, Arizona, United States
$55k-$65k/yr OnsiteFull Time
Execute study activities from startup through closeout in compliance with GCP and sponsor standards; conduct patient visits, maintain source documents, process samples, and communicate with sponsors and vendors.
EDC, EMR, Microsoft Excel, Microsoft Word, Microsoft Outlook
1mo
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Clinical Research Coordinator I - Strong Heart Study - Phoenix, Arizona
Phoenix, Arizona, United States
$49k-$87k/yr OnsiteFull Time
1+ YOE1-2 years clinical research experience, high school diploma required (bachelor's or allied health degree preferred); experience in healthcare and working with tribal communities desired; regulatory, consent, and biospecimen handling skills.
Clinical Trial Management System (CTMS)
2w
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Clinical Research Coordinator II, Department of Internal Medicine – Cardiology (Phoenix)
Phoenix, Arizona, United States
$53k-$66k/yr OnsiteFull Time
3+ YOEBachelor's degree plus 3 years relevant experience; conduct recruitment/consent, coordinate study procedures, specimen handling per IATA, data entry and quality checks, ensure regulatory compliance.
EDC, IATA, electronic health record
1mo
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Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Phoenix or Detroit or Boston or Charlotte or Chicago or Seattle or Cincinnati or Irving or Salt Lake City or Houston
RemoteFull Time
1+ YOEBachelor's in health/science, 1+ year CRC experience, valid driver's license, ability to travel 60-70% nationwide, Microsoft Office proficiency, strong communication and attention to detail.
Microsoft Office
3w
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Clinical Project Coordinator
Tempe, Arizona, United States
OnsiteFull Time
1+ YOEBachelor's in life sciences or equivalent,1+ years clinical research experience,proficiency with Microsoft Suite,experience with study supply management/shipments,strong communication,organizational and critical thinking skills.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft OneNote, Microsoft To-Do, Microsoft SharePoint, eTMF, CTMS, CDMS, Veeva Vault
6d
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Clinical Administrative Coordinator
Dallas or Hartford or Minneapolis or Phoenix or Tampa
$18-$32/hr RemoteFull Time
2+ YOEHigh school diploma/GED or equivalent experience, 2+ years in healthcare, medical claims processing or research, Microsoft Word, Outlook and Adobe PDF experience, and medical terminology familiarity.
Microsoft Word, Microsoft Outlook, Adobe PDF, ICD-10, CPT, UNET, CPA/Cosmos, CSP/Facets, Cirrus/USP, UHCW/NICE
2mo
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Clinical Study Coord
Duarte or Los Angeles or Orange County or Atlanta or Chicago or Phoenix
OnsiteFull Time
2+ YOEBachelor's in science/health preferred (substitutable by additional experience). Minimum 2 years research or clinical experience. Must obtain ACRP or SOCRA within 1 year; IATA, GCP, HSP, and BLS within 1 month. Understand/apply FDA, OHRP, GCP/ICH, HIPAA; execute protocols; coordinate recruitment/consent; monitor participants and report adverse even...
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