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CALHN Research Director

Ethics

  • CALHN HREC
  • HREC submissions
  • National Mutual Acceptance (NMA)
  • Research GEMS Human Research Ethics Application (HREA)
  • HREC invoicing and fees

Governance

  • Research GEMS
  • Investigator Initiated Site Specific Assessments (SSA)
  • Agreements

Low risk

Quality assurance page:

  • Quality Improvement (QI)
  • Audits

Low risk page:

  • Low Risk Project Submissions
  • Expedited Review Panel (ERP)
  • Case Reports
  • Publications
  • Triggers for Ethical Review

Monitoring

  • Post-Approval Monitoring Submissions
  • Progress Report
  • Final/Site Closure Reports
  • Amendments
  • Serious Breaches, Suspected Breaches and Deviations
  • Safety Reporting

Clinical trials

  • Confidentiality Disclosure Agreements (CDAs)
  • Clinical Trial Research Agreements (CTRAs)
  • Commercially Sponsored Site-Specific Assessments (SSA)
  • Clinical Trial Notification Scheme (CTN)
  • Clinical Trial Approval Scheme (CTA)
  • Clinical Trial Invoicing
  • Clinical Trial Facilities and Research Unit Information

Clinical trial accreditation

Grants

  • Internal and external grant applications
  • Variations
  • Progress reports
  • Grant revenue invoicing

HSCGB and internal grants

  • Health Services Charitable Gifts Board (HSCGB) 
  • Internal grants
  • Scholarships
  • Fellowships
  • Grants and awards 

Research finance

  • Budgets
  • Special Purpose Fund (SPF) creation

RAH Research Fund

  • Philanthropy
  • Donations
  • Funding

Clinicians PhD Pathway (CPP)

  • Mentorship
  • Guidance
  • Specialist training

PARC clinical research

  • Recruitment
  • Education and training
  • Study monitoring
  • Nursing
  • Technical and laboratory
  • Consultancy

Adelaide EpiCentre

  • Health informatics
  • Biostatistics
  • Health economics
  • Epidemiology centre

This page was last updated 29 May 2025.

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