Clinical Research Associate — Hybrid & Global Trials

IQVIA; Sydney; Hybrid; AUD 70,000 - 110,000; Full time

Benefits offered by this job

Flexible hybrid work

Car and health allowances

Career growth opportunities

Job summary

IQVIA is seeking a Clinical Research Associate in Australia to monitor sites and manage trial activities in compliance with GCP/ICH guidelines. The role supports recruitment strategies, site training, and data quality across multiple Australian locations, with a flexible hybrid work setup.

The position engages with study teams, maintains regulatory documents, and ensures site performance aligns with sponsor requirements, offering visa sponsorship for eligible candidates.

Qualifications

• Bachelor's degree in science or health care.
• Minimum 9 months of independent on-site monitoring experience.
• GCP and ICH guidelines knowledge and application.
• Proficient in MS Word, Excel and PowerPoint.

Responsibilities

• Perform site monitoring visits in accordance with GCP/ICH and scope of work.
• Collaborate with sites to drive subject recruitment per project needs.
• Administer protocol training and maintain regular site communication.
• Assess site practices for protocol adherence and regulatory compliance.
• Track regulatory submissions, enrollment, CRF completion, and data queries.
• Ensure TMF/ISF documents are maintained per regulatory requirements.
• Create visit reports and follow-up correspondence; liaise with study team.
• Support site start-up and overall study execution as needed.

Skills

On-site monitoring

GCP/ICH knowledge

Regulatory knowledge

Bachelor's degree in science/health

MS Office proficiency

Time management

Communication skills

Education

Bachelor's Degree in scientific discipline or health care

Tools

MS Word

MS Excel

MS PowerPoint

Laptop

iPhone

iPad

Job description

IQVIA is seeking a Clinical Research Associate in Australia to monitor sites and manage trial activities in compliance with GCP/ICH guidelines. The role supports recruitment strategies, site training, and data quality across multiple Australian locations, with a flexible hybrid work setup.

The position engages with study teams, maintains regulatory documents, and ensures site performance aligns with sponsor requirements, offering visa sponsorship for eligible candidates.