Clin Res Assoc I

Job Location(s) AU-Sydney
Job Number
Job Category
Clinical Research Associates
Position Type

Job Overview

Job Overview:
Do you have 6-12 months monitoring experience?  Would you like to gain broader experienced working on multiple studies for various sponsors?  Look no further!
♦ Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance  liaise with vendors 
♦ Responsible for aspects of registry management as prescribed in the project plans
♦ General On-Site Monitoring Responsibilities
$70, 000 to $75, 000 plus $18, 575 car allowance


Minimum Required:
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
- Basic knowledge of Regulatory Guidelines
- Basic understanding of the clinical trial process
- Fluent in local office language and in English, both written and verbal
- Working knowledge of Covance SOPs regarding site monitoring


Minimum Required:
- Six (6) months experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc.)
- Basic understanding of Regulatory Guidelines
- Ability to work within a project team
- Good planning, organization and problem solving skills
- Good computer skills with good working knowledge of a range of computer packages
- Works efficiently and effectively in a matrix environment
- Valid Driver's License
- One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
- 6 months on site monitoring experience


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