Remote CRA II - Clinical Trials Monitoring & Integrity

ICON Clinical Research; Melbourne; Hybrid; AUD 70,000 - 90,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee Assistance Program (LifeWorks

Life assurance

Flexible benefits

Job summary

ICON Clinical Research in Melbourne, Australia is seeking a CRA II to design and monitor clinical trials in a sponsor‑dedicated framework. This role involves interpreting complex data, ensuring safety and data integrity, and collaborating with investigators to execute studies.

The position supports remote work options within Australia and requires a willingness to travel up to ~60%, with responsibilities across site qualification through close-out visits.

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

• Conduct site qualification, initiation, monitoring and close-out visits.
• Ensure protocol compliance, data integrity and patient safety.
• Collaborate with investigators and site staff to enable study conduct.
• Review data and resolve queries to maintain quality data.
• Assist with preparation and review of study documents including protocols and CSRs

Skills

Clinical monitoring

ICH-GCP knowledge

Organizational skills

Communication skills

Independent worker

Travel willingness

Education

Bachelor's degree in science/healthcare

Job description

ICON Clinical Research in Melbourne, Australia is seeking a CRA II to design and monitor clinical trials in a sponsor‑dedicated framework. This role involves interpreting complex data, ensuring safety and data integrity, and collaborating with investigators to execute studies.

The position supports remote work options within Australia and requires a willingness to travel up to ~60%, with responsibilities across site qualification through close-out visits.