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 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 cutting-edge 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,