
Clinical Research Associate II
Precision Medicine Group
full-time
Posted on:
Location Type: Remote
Location: Australia
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About the role
- The CRA II provides overall support to study sites and clinical project teams engaged in clinical research studies.
- Oversees all aspects of study site management to ensure patient safety is protected.
- Provides guidance at the site and project level towards audit readiness standards.
- Updates, tracks and maintains study specific trial management tools/systems, and status reports.
- Independently conducts all forms of site visits, including pre-study/qualification, initiation, routine monitoring, and close-out visits.
- Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents.
- Communicates effectively and proactively with both site personnel and Precision Project and Clinical Trial Management.
Requirements
- Bachelor's degree / international equivalent or equivalent combination of education and experience ideally in a business, scientific or healthcare discipline.
- Minimum of 2 years of on-site monitoring experience; 1 year oncology and Phase I experience preferred
- High in proficiency in the Microsoft Office package of programs (Outlook, Word, Excel, and PowerPoint).
- Customer service demeanour; demonstrate flexibility and teamwork.
- Ability to focus on detail for extended periods of time, high attention to accuracy.
- Fluency in English communication, verbally and in writing.
- Working knowledge of the drug development process.
Benefits
- Competitive salary
- Health insurance
- Professional development opportunities
- Remote work options
- Paid time off
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
on-site monitoringclinical researchaudit readinesstrial management toolsdocumentationattention to detaildrug development process
Soft Skills
customer serviceflexibilityteamworkcommunicationaccuracy