Experience

Auctus Training & Education RTO 40879

• Australia
• Professional Training and Coaching
• 1 - 100 Employee

• Project Officer

  • Jan 2023 - Present

  Coordinating and assessing RPL for Certificate III in Individual Support

• Trainer and Assessor

  • Mar 2018 - Present

  Registered Nurse - Training:Certificate III in Individual SupportFirst Aid HLTAID011Assist with MedicationConsulting in IndustryContinuous Improvement of course materials



Motor Neurone Disease Association of South Australia (MND SA)

• Australia
• Hospitals and Health Care
• 1 - 100 Employee

• MND Advisor

  • Nov 2014 - Mar 2018

  Provision of Motor Neurone Disease (MND) specific information and advice to clients and their families Identify community supports and services and make appropriate referrals Support clients within the NDIS or via My Aged Care Provision of Augmentative and Alternative Communication and education on use Continued ongoing support to clients and families via home visits or phone support Provision of information, training and education on MND and symptom management to other service providers Advocate on behalf of people living with MND and collaborate with other service providers and health care professionals Liaising with researchers, specialists and nurses with projects Event Planning and Coordination Data collection for Australian Motor Neurone Disease Registry Show less



SAHMRI

• Australia
• Research
• 200 - 300 Employee

• Clinical Trial Coordinator

  • Dec 2011 - Nov 2014

  Conduct trials in accordance with the agreed protocols and ICH GCP guidelines Comply with required standard procedures and policies while maintaining confidentiality and security of patient information Collaborate with the Principal Investigator and other departments as required for the implementation and continuation of the trial Complete ethics committee and governance submissions Ensure adherence to the protocol and document breaches or violations by notifying the Sponsor and the Ethics Committee Immediate reporting of Serious Adverse Events and Adverse events as required by the Sponsor, Ethics Committee and relevant clinical guidelines Develop documents, letters, regulatory files and CRFs as needed for the trial Screen and provide screening logs Enrol subjects into trials and provide follow up visits as per schedule Specimen collection, BP monitoring, trial medication organisation Show less