VIRTUAL WORKSHOP
*NEW workshop
Clinical Research Associate (CRA) Accelerate
“The CRA workshop was thoughtfully designed, providing a thorough and comprehensive overview of all the aspects I needed to learn. The teaching methods and presentations were engaging and kept me fully involved throughout the entire session. I appreciated how the material was delivered in a way that maintained my focus and energy, ensuring that I never felt tired or lost concentration.
This workshop is incredibly useful for anyone working in clinical trials, regardless of their role—whether you’re a coordinator, an associate, or at any other level. It offered me a fresh perspective on my work, allowing me to view my responsibilities from a new angle and inspiring me to grow. I highly recommend it to others.”
Narges Janalizadeh ,Study Start-Up Specialist from NHW
“The facilitator had great knowledge of the content. It was a great overall look into the life of a CRA. Fantastic interactive workshop.”
Michelle Shaw, Clinical Trials Assistant, SAHMRI Clinical Trials Platform.
The only training of its kind for CRAs in Australia, PRAXIS have just released a new training solution to help expand your skillset as a CRA.
As a leading Australian and international education provider, PRAXIS Australia have developed a cost-effective and 100% online Clinical Research Associate (CRA) Accelerate workshop. This workshop is specifically designed to strengthen your confidence and capacity in your daily work by providing you with the latest knowledge in key areas of your role.
You will gain knowledge in research monitoring, ethics, and good clinical practice, allowing you to supervise the initiation and execution of clinical trials projects, on behalf of sponsor organisations.
You can claim 4 CPD points from this workshop.
Who is this workshop for?
- Health Science graduates
- Staff (medical, nursing, biomedical science, or allied health) who are pursuing a career in clinical research as a Clinical Research Associates (CRA)
What will you learn?
On completion, you will be able to:
- Explain how high ethical standards and data quality are maintained in research
- Describe requirements and processes for research monitoring, audit and participant safety reporting
- Describe the importance of participant informed consent and outline the process
- How to control and reduce risk, and safety reporting requirements for Investigators and Sponsors.
Our training and education offers have been developed according to Australian and international best practice standards.
Our modules are built upon the competencies developed by the Harvard Multi-Regional Trials Centre (MRCT) and aligned to competencies recommended by the NHMRC.
These training offers are regarded as a benchmark for researchers, clinical trials, and healthcare professionals in Australia and internationally.
Facilitator
Michelle Tusler
Michelle is a clinical research professional with 15+ years’ experience in multiple clinical research roles within pharmaceutical companies and CROs with national and international project management experience.
Currently the Head of Clinical Operations at an Australian based CRO, Michelle specialises in supporting small to medium biotech companies in their drug development pathway.
Passionate about quality training and oversight management for Sponsors and also Site Responsibilities, Michelle has implemented major Clinical Trial Management Systems (CTMS) and been part of Risk Based Monitoring development across multiple companies.
Michelle is a qualified auditor in ISO 9001:2015 and has a keen interest in developing quality systems in relation to delivering clinical research to a high standard.
Price
$599pp plus GST
*Savings available for group enrolments and for PRAXIS partner organisations.
Next Virtual Workshop
Thursday 12 June 2025: 10.00am – 14.00pm AEST
Need training on demand?
This session can also be conducted at your location for groups of 10 or more. Ask us about this today.
PRAXIS Australia has the right to cancel a training session (or move the event format online) due to unforeseen circumstances such as low registration/attendance numbers or changes in Government restrictions surrounding the ongoing COVID19 pandemic. For more information regarding our Cancellation Policy and your rights, please see our Student Terms and Conditions.
Suggestion box: new offers and interest areas
What would you like to see from us? This can be a topic we haven't covered yet, a course style, or a different way of delivering our courses and workshops. All suggestions are welcome and will be considered.