CRA II - Melbourne, Australia Remote
At ICON Strategic Solutions, you will work in a sponsor‑dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative workplace where your work contributes to the development of treatments that benefit patients worldwide. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:
+ Conducting site qualification, initiation, monitoring, and close‑out visits for clinical trials.




+ Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
+ Collaborating with investigators and site staff to facilitate smooth study conduct.
+ Performing data review and resolution of queries to maintain high‑quality clinical data.
+ Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Your Profile:
Required qualifications and experience:
+ Bachelor's degree in a scientific or healthcare‑related field.
+ Minimum of 2 years of experience as a Clinical Research Associate.
+ In‑depth knowledge of clinical trial processes, regulations,

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