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Clinical Research Associate (Home-based, Brisbane)

medpace•Australia•🌍 Remote
Full-timefresher
👁️ 0 views•📝 0 applications•Posted 10/22/2026•Expires 12/21/2026
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Job Description

What can Medpace offer you?

Flexible working conditions – Opportunity to work from home and flexible working hours Visa sponsorship & transfer for qualified candidates already based in Australia Competitive transportation allowance Annual Merit increases Variable Compensation Bonus Plan – Lucrative bonus calculated directly from the number of visits you do MEDPACE CRA TRAINING PROGRAM (PACE®) No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.

Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence:

• PACE®provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.

• PACE®will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.

To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process. No metric for minimum required days on site per month.

Opportunity for cross-functional and CRA leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager Airline club allowance Casual Dress Code Responsibilities Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians and their site staff; Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations approp

Required Skills

clinical researchmonitoringdocumentationprotocol compliancecross-functional leadershipclinical trial management

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