Full-Time

IRB Coordinator 2

Research Office

Medical College of Wisconsin

Medical College of Wisconsin

No salary listed

Wisconsin, USA

Hybrid

Hybrid role; some on-site days in Wisconsin.

Category
Biology & Biotech (1)
Requirements
  • Minimum Required Education: Bachelor’s degree
  • Minimum Required Experience: 3 years
  • Required Certification/Licensure(s): CITI within 90 days of hire
  • Appropriate experience may be substituted for education on an equivalent basis.
  • Knowledge of biology, chemistry, mathematics, documentation, and records management.
  • Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Responsibilities
  • Assigned to one or more IRBs, review protocols, amendments, protocol deviations, serious adverse events, and continuing progress reports.
  • Consult with research coordinators and investigators to provide suggestions for improvements and modifications to submissions.
  • Provide professional service to the Chair, IRB Committee, and clinical investigators which involve the application of established principles, theories and concepts.
  • Resolve moderately complex issues involving more advanced research into ethical questions.
  • Consult with the IRB chair to determinemostappropriate course of action for review.
  • Conduct meeting preparation, and meeting follow-up for human subject protocols.
  • Draft Standard Operating Procedures for newly creating or existing processes.
  • Prepare approval letters for signature and other appropriate documents.
  • Prepare study related documents for review by Chair and/or committee.
  • Review submitted documents for accuracy and completeness as per IRB regulations.
  • Other duties as assigned.
Medical College of Wisconsin

Medical College of Wisconsin

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