Associate Devops Engineer (Remote Optional)

Junee Southern Cross; Gold Coast City; Hybrid; AUD 90,000 - 110,000; Full time

Job summary

ICON Strategic Solutions is seeking a CRA II in a hybrid arrangement based in Australia. The role involves site qualification, initiation, monitoring and close-out visits, ensuring protocol compliance, data integrity, and patient safety throughout trials.

Vous will collaborate with investigators and site staff to facilitate study conduct, perform data review, resolve queries, and contribute to study documentation including protocols and clinical study reports.

Responsibilities

• 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

Job description

CRA II - Hybrid, Australia
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
As the world's largest FSP organization, 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 analyze clinical trials, interpreting complex medical data and contributing to the advancement of innovative treatments and therapies.
What You Will Do:
+ 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