Senior Clinical Research Associate — Flexible Hybrid CRA

IQVIA; Melbourne; Hybrid; AUD 105,000 - 145,000; Full time

Benefits offered by this job

Car allowance

Health allowance

Job summary

IQVIA is seeking a Clinical Research Associate to monitor and manage study sites across multiple Australian trials. You will ensure adherence to protocol, GCP, and regulatory requirements while coordinating with site staff to drive data quality and timely reporting.

The role requires on-site visits, clear communication, and strong organizational skills. A hybrid setup with a Melbourne office supports career growth within our global CRO network.

Qualifications

• Bachelor's degree in scientific discipline or health care
• At least 9 months of independent on-site monitoring experience
• Equivalent combination of education, training and experience may be accepted
• Good knowledge of GCP and ICH guidelines
• Proficient in Word, Excel and PowerPoint; able to use mobile devices as applicable

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope and regulatory requirements (GCP/ICH)
• Drive subject recruitment plans with sites to enhance predictability
• Administer protocol training to sites and maintain regular communication
• Evaluate site practices for protocol and regulatory compliance; escalate issues
• Track regulatory submissions, recruitment, CRF completion, data query resolution; may support start-up
• Maintain site documents and TMF/ISF in compliance with GCP/regulations
• Collaborate with study team for project execution
• Support development of project recruitment plans per site
• Manage site financials per trial agreement and invoice retrieval as required

Skills

On-site monitoring

Regulatory knowledge

Communication

Organizational skills

Problem solving

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Laptop

iPhone/iPad

Job description

IQVIA is seeking a Clinical Research Associate to monitor and manage study sites across multiple Australian trials. You will ensure adherence to protocol, GCP, and regulatory requirements while coordinating with site staff to drive data quality and timely reporting.

The role requires on-site visits, clear communication, and strong organizational skills. A hybrid setup with a Melbourne office supports career growth within our global CRO network.