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Clinical Research Coordinator II

University of Arizona

Tucson, AZ

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JOB DETAILS
SKILLS
Adverse Events, Biological Processes, Chain of Custody, Clinical Laboratory, Clinical Research, Clinical Trial, Communication Skills, Conduct Studies, Data Collection, Data Entry, Database Administration, Documentation, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Maintain Compliance, Operations Research, Organizational Skills, Quality Control, Regulations, Regulatory Requirements
LOCATION
Tucson, AZ
POSTED
18 days ago
  • Coordination of study visits and study procedures. Maintaining regulatory and study documentation.
  • Creating source documents, study specific training in accordance with study protocols and Good Clinical Practice (GCP) guidelines.
  • Perform participant pre-screening, screening, recruitment, enrollment, and informed consent.
  • Conduct study visits and clinical procedures as required by protocol.
  • Maintain accurate and complete source documentation and study records.
  • Develop study-specific tools including source documents, visit checklists, and training materials.
  • Ensure maintenance and organization of regulatory documentation, including IRB submissions, continuing reviews, protocol amendments, and reporting requirements.
  • Monitor and report adverse events, serious adverse events, and protocol deviations in accordance with institutional and sponsor requirements.
  • Perform data collection, entry, management, and quality control checks to ensure accuracy and completeness of study data.
  • Resolve data queries and maintain research databases (e.g., REDCap or equivalent systems).
  • Work closely with Principal Investigators to coordinate and execute all aspects of multiple clinical trials.
  • Collect, process, and ship biological specimens according to protocol requirements and ensure proper chain of custody and storage conditions.
  • Maintain study supplies, inventory, and equipment required for research operations.
  • Communicate effectively with study sponsors, IRB, clinical teams, laboratories, and other stakeholders to ensure study compliance and efficiency.
  • Participate in study initiation, monitoring visits, audits, and close-out activities as required.
  • Responsibilities are subject to change based on departmental priorities, study requirements, regulatory obligations, and operational needs.

About the Company

U

University of Arizona