CRA II - Melbourne, Australia RemoteAt 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 cooperative environment 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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