Training and Education
for the New Zealand Private Sector
PRAXIS Australia is excited to announce a unique opportunity for New Zealand staff involved in, or aspiring to work within the clinical trials and research sector in New Zealand.
The New Zealand Research Essentials courses have been specifically adapted and updated to suit the needs of the New Zealand sector, and are developed in partnership with Health New Zealand | Te Whatu Ora.
Materials have been customised to the NZ regulatory environment and to Treaty of Waitangi and cultural safety awareness.
Research Essentials modules are built upon the competencies developed by the Harvard Multi-Regional Trials Centre (MRCT) and aligned to competencies recommended by the National Health and Medical Research Council (NHMRC). These training offers are regarded as a benchmark for researchers, clinical trials, and healthcare professionals internationally.
Once you have successfully registered you will receive an email from PRAXIS within 1-2 business days with further enrolment instructions.
- All PRAXIS modules are online, flexible and self-paced.
- All modules completed are eligible for four Continuing Professional Development (CPD) points, which may be used for maintaining relevant registrations.
- Modules can be completed within 12 months of enrolment.
Module Options
(Please select as many modules as you wish)
Good Clinical Practice
- C5.01 New Zealand Good Clinical Practice (ICH-GCP)
Research Development and Publication
- C1.02 Identifying and Formulating Research Questions
- C1.03 Evidence in Research
- C1.04 Differentiating Research from Innovation, Clinical Care, Audit and QA
- C1.05 Research Design and Methods
- C1.06 Designing a Research Proposal
- C6.06 Skills for Getting Published
Research Ethics, Governance and Cultural Safety
- C2.06: An Introduction to Cultural Safety in Research
- C2.10 Consent to Research
- C5.07 Research Integrity and Research Misconduct
- EC.04 Principles of Research Governance
Research Operations
- C3.02 Principles of Project Planning
- C3.06 Essential Documentation in Clinical Trials
- C3.07 Quality Assurance for Clinical Trial Sites
Completion time: Estimated completion is up to 4 hours per module.