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 cooperative 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 creative 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,
J-18808-Ljbffr