Terms of Reference
Objectives and Responsibilities
- To be responsible for the overall scientific review of clinical study proposals and associated ethics applications, publication, dissemination and implementation of study outcomes.
- Ensure the services provided by PaCCSC are aligned with the principles of Good Clinical Practice and the PaCCSC’s standard operating procedures.
- To advise the Management Advisory Board on:
- The suitability of a protocol from the scientific viewpoint and preparation for submission to research ethics committees
- Recommendations for changes that will facilitate a protocol or a submission in proceeding to the next stage
- The suitability of the draft final version of a protocol for submission to research ethics committees.
- Determine that trial design is aligned with TGA guidelines and PBAC requirements and will produce evidence which may also assist with:
- Clinical decision making
- Improvement in clinical care
- Health policy and funding requirements.
- To oversee and receive regular reports from the Publications Subcommittee and from time-to-time to make decisions referred to it by the Publications Subcommittee.
- To revise these Terms of Reference as deemed appropriate.