8 irb jobs at 7 companies in Phoenix, AZ
2w
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Lead Clinical Research Coordinator
Sun City, Arizona, United States
OnsiteFull Time
3+ YOEManage clinical study operations, ensure protocol and GCP compliance, oversee data integrity, mentor coordinators, prepare IRB submissions, and support audit readiness.
REDCap, Medidata, Microsoft Word, Microsoft Excel, Microsoft Outlook
4d
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Clinical Research Assistant (31960)
Peoria or Anthem or Glendale or Glendale or Litchfield Park or Sun City West
OnsiteFull Time
1+ YOE>1 year medical or research assistant experience, knowledge of GCP/ICH/FDA/IRB rules, EMR and data systems proficiency, strong communication and time-management skills.
Microsoft Office, EMR, EDC, IVRS, Practice Management
3w
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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 Assistant (CRA)
Gilbert, Arizona, United States
$38k-$48k/yr OnsiteFull Time
1+ YOEBachelor's degree in a related field, 1+ years clinical research experience (psychiatry/CNS preferred), phlebotomy certification, knowledge of GCP/IRB/FDA processes, strong documentation and communication skills.
EDC, CTMS, CRIO, EMA Wellness
1w
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Coordinator - Research Engagement
Scottsdale, Arizona, United States
OnsiteFull Time
2+ YOEBachelor's in related field or equivalent, minimum 2 years healthcare/research coordination experience, strong organization, knowledge of clinical research/IRB basics, Microsoft Office and tracking system proficiency.
Microsoft Office Suite, CTMS
1w
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Research Program Manager - Investigator Initiated Studies
Scottsdale, Arizona, United States
OnsiteFull Time
3+ YOEBachelors in life/health science required; 3+ years clinical research/program coordination; knowledge of FDA/GCP/IRB; grant and protocol experience; preferred CCRC/CCRA/PMP and advanced degree.
CTMS, Grants.gov, eRA Commons
2mo
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Clinical Study Documentation Specialist
Phoenix, Arizona, United States
OnsiteFull Time
2+ YOEAssociates degree; 2 years IRB document submission; strong clinical research documentation; proficient in Microsoft Office and regulatory systems; strong organization; able to manage multiple studies; background checks required.
Microsoft Office, IRB portals, CTMS, Regulatory systems
1mo
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Human Factors Lead Research Scientist
Phoenix, Arizona, United States
HybridFull Time
6+ YOE6+ years human factors research experience in aerospace or related high-tech domain, 1+ year industry experience, ability to design/execute studies, author IRB and technical documentation, and analyze results using tools like R, SPSS, MATLAB, or Python.
R, SPSS, MATLAB, Python