Clinical Research Coordinator

ZimZee Recruiting

Lehi, UTFull-timePosted Apr 25, 2026

Behavioral Health Market Context

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Qualifications

  • 5-8 years of experience supporting or leading clinical research studies in regulated healthcare or laboratory environments
  • Strong knowledge of IRB processes, human subjects research requirements, and informed consent procedures
  • Hands-on experience coordinating clinical study documentation and protocol execution
  • Proficiency with clinical study tracking platforms or regulatory submission systems (e.g., WCG or similar)
  • 1 more items(s)

Responsibilities

  • The Coordinator will support the execution of clinical research protocols through hands-on coordination of study operations, laboratory instrumentation, regulatory documentation, and cross-functional communication
  • The ideal candidate brings strong experience in clinical research environments, familiarity with IRB-regulated studies, and the ability to manage multiple active protocols simultaneously
  • Familiarity with laboratory instrumentation support, QC procedures, and preventive maintenance coordination
  • Experience maintaining regulatory documentation and source files in compliance with SOPs
  • Strong coordination skills working with clinical leadership, nursing staff, and external vendors
  • Experience troubleshooting instrument or study workflow issues and escalating when appropriate
  • Coordinate execution of clinical study protocols, ensuring documentation completeness, regulatory compliance, and operational readiness
  • Manage clinical and laboratory instrument readiness, including QC procedures, supply coordination, and preventive maintenance scheduling
  • Obtain and manage informed consent documentation in accordance with human subjects research requirements
  • Serve as a liaison between clinical leadership, IRB stakeholders, and internal teams to support study progress and regulatory alignment
  • Maintain accurate study documentation, upload source materials, and ensure proper digital record organization across systems
  • Support study scheduling logistics with nursing staff and ensure staffing availability aligns with protocol requirements
  • Monitor protocol status, communicate risks or deviations, and provide updates to clinical leadership on study progress
  • 10 more items(s)


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