Overview
We're looking for a Clinical Research Associate 2 who's ready to take their career to the next level—working on cutting-edge studies that shape the future of medicine. Ideally based in Sydney or Melbourne. Positions available in our Core and Single sponsor team. As part of the assessment, you may be asked to complete a short video screening interview.
Responsibilities
Engage in Site Visits: From selection to close-out, visits are pivotal in ensuring the success of our studies.
Recruitment Strategies: Develop and implement plans to recruit study subjects, impacting project outcomes.
Empower Sites with Knowledge: Provide essential training and maintain robust communication to keep sites aligned and motivated.
Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
Drive Study Progress: Monitor regulatory submissions, data query resolutions, and overall study execution.
Master Documentation: Maintain meticulous records and site documents.
Collaborate and Innovate: Work with a team to support project execution and drive success.
Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval.
Qualifications
A degree in life sciences or healthcare (or equivalent experience).
18 months minimum on-site independent monitoring experience, ideally oncology.
Deep knowledge of GCP, ICH, and clinical trial operations.
Tech-savvy with Microsoft Office and mobile tools (iPhone/iPad).
Proactive mindset, strong communication skills, and a passion for excellence.
Why Join Us
Work on diverse, global studies across multiple therapeutic areas.
Be part of a supportive, innovative team that values your growth.
Flexible work arrangements, travel opportunities, and career development.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. Learn more at
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