Remote Mortgage Credit Analyst — Complex Lending Specialist

Blue Collar Money; Sydney; Remote; AUD 70,000 - 95,000; Full time

Job summary

ICON Strategic Solutions in Melbourne is seeking a CRA II to contribute to clinical trial monitoring and data analysis in a sponsor‑dedicated model. The role involves site visits, ensuring protocol compliance, data integrity and collaboration with investigators to advance treatments globally.

The position requires a Bachelor’s in a scientific/healthcare field and at least 2 years as a CRA, with deep knowledge of clinical trial processes and regulations.

Qualifications

• 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.

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.

Skills

Clinical trial knowledge

Regulatory knowledge

Data review

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

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 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,