Discover a series of online learning modules each providing information, resources and scenarios explaining the key fundamental activities of clinical trials.
There are currently seven online modules for the emerging clinical trial workforce in Victoria:
Feasibility to ethics approval
Governance to site initiation
From screening to participant enrolment
Managing a participant on a trial
From initiation to close-out
Problem-solving in clinical trials
Teletrial approach: a flexible way to conduct clinical trials to overcome geographical barriers.
Upskill the clinical trials workforce to effectively run clinical trials utilising good clinical practice.
Facilitate compliance with the requirements of the research protocol and good clinical research practice
Identify the financial and resource variables that affect trial start up and ongoing conduct
Ensure patient comprehension and safety during initial and ongoing clinical trial informed consent discussions.
Apply a variety of resources and strategies to manage the care of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and management of symptoms
Ensure collection of source data and completion of documentation that validate the integrity of the conduct of the clinical trial
Ensure adherence to ethical practices and regulations during the conduct of clinical trials to protect the rights and well-being of patients and the collection of quality data.
Clinical trial study team (PIs, SCs, RNs, CTAs) novice to intermediate level.
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