Clinical Research Associate (CRA) – Sydney

About the role

ICON is seeking a Clinical Research Associate (CRA) in Sydney to support sponsor‑dedicated clinical trials. You will work within ICON’s global network, contributing to the design, monitoring and analysis of studies that advance innovative therapies.

Key responsibilities

• Conduct site qualification, initiation, monitoring and close‑out visits for assigned clinical trials.
• Ensure protocol compliance, data integrity and patient safety throughout the study lifecycle.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review, resolve queries and maintain high‑quality clinical data.
• Assist in preparation and review of study documentation such as protocols and clinical study reports.

Required profile

• Bachelor's degree in a scientific or healthcare‑related field.
• Minimum of 2 years experience as a Clinical Research Associate.
• Strong organizational and communication skills with attention to detail.
• Ability to work independently and collaboratively in a fast‑paced environment.
• Willingness to travel up to 60% of the time.

Required skills

• In‑depth knowledge of clinical trial processes and regulations.
• Familiarity with ICH‑GCP guidelines.
• Experience in data review and query resolution.
• Protocol compliance and patient safety monitoring.

What we offer

• Competitive base salary and performance‑related incentives.
• Health, dental and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.