Priority area action and activity timeline
Short-term (<2yrs)
Medium-term (2-4yrs)
Long-term (>5yrs)
Activity
Priority Area 3: ENABLE – Strengthen the enablers of our research
3.1 Enable workforce research capacity.
Establish protected time for clinician researchers, and develop career pathways for clinical research operations staff.
Provide targeted training, workshops, and mentoring programs for new and early-career researchers.
Enable access to pooled support roles (e.g. clinical trial coordinators, biostatisticians) for teams with limited capacity.
3.2 Streamline ethics and governance processes to enable timely clinical trial and research activity.
Foster stronger linkages between the research governance and clinical governance teams to ensure clear pathways exist for QA, QI and research.
Establish a pre- submission support service to ensure faster approval timelines for both ethics and governance submissions.
Ensure training and resources on ethics and governance processes are available to all staff.
3.3 Enhance access to high-quality health data for clinical trials, research and quality improvement.
Pilot SDPR-enabled systems to enhance data use for research and quality improvement.
Develop and support data sandboxes and safe platforms for researchers to analyse data.
Embed bioinformatics expertise across the district to support research and clinical trials.
Improve data governance clarity and navigation (e.g. processes, custodianship, access pathways).
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The logos linked to each guiding principle are reflected through the associated actions.
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