CRA II - Clinical Trial Monitoring & Data Integrity

KCR Placement

Sydney

On-site

AUD 90,000 - 120,000

Full time

2 days ago

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Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to support sponsor-dedicated trials across New South Wales, Queensland, and South Australia. You will design and analyze clinical trials, interpreting complex medical data to help advance treatments for patients worldwide.

You will conduct site qualification, initiation, monitoring and close-out visits, ensure protocol compliance, data integrity, and patient safety, collaborate with investigators, review data queries, and

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, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.
Ability to work independently and collaboratively in a fast-paced environment.
Willingness to travel as required (approximately 60%)

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