- SalaryGreat Hourly rate
- LocationMacquarie Park
- Job type Part Time
- DisciplineClinical Research
- ReferenceBH-40044-1
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Clinical Trial Assistant
Job description
Benefits
About the company
Join a global medical device company, with an innovative and forward thinking approach to the healthcare industry specialising in unique and market leading products. A company driven to progress and continuously strive for success whilst maintaining commitment to their customers and ensuring a positive patient outcome.
About the opportunity
The Clinical Trials Assistant will assist in the coordination and administration of the study activities and within the Study teams to ensure quality and consistency of the study deliverable to time, cost, and quality objectives.
Duties
Skills and Experience
Culture
Close knit team that are open and collaborative. Looking for someone with a can do attitude that will be able to use their initiative to support the team
How to Apply
Click apply or contact Davina Ocansey, Senior Recruitment Consultant on +61 2 8877 8712 for a confidential discussion.
- 12 month contract – 3 days a week
- Work with a leading medical device company
- Close knit and supportive team
About the company
Join a global medical device company, with an innovative and forward thinking approach to the healthcare industry specialising in unique and market leading products. A company driven to progress and continuously strive for success whilst maintaining commitment to their customers and ensuring a positive patient outcome.
About the opportunity
The Clinical Trials Assistant will assist in the coordination and administration of the study activities and within the Study teams to ensure quality and consistency of the study deliverable to time, cost, and quality objectives.
Duties
- Assist in coordination and administration of clinical studies from the start-up to execution and close-out.
- Interface with Investigators, external service provider and CRAs during the collection process to support effective delivery of a study and its documents.
- Contribute to electronic applications/submissions by handling clinical-regulatory documents according to the requested technical standards
- Set-up, populate and accurately maintain information in tracking and communication tools
Skills and Experience
- Working knowledge and understanding of clinical research including: CTMS, EDC and SOPs
- Invoice / payment management experience
- Computer proficiency
- Minimum 1 year experience as a CTA
- Very good knowledge of spoken and written English
- Good interpersonal skills and ability to work in a team environment
- Display excellent organisation and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting priorities
Culture
Close knit team that are open and collaborative. Looking for someone with a can do attitude that will be able to use their initiative to support the team
How to Apply
Click apply or contact Davina Ocansey, Senior Recruitment Consultant on +61 2 8877 8712 for a confidential discussion.