Hybrid Clinical Research Associate – Flexible Work & Perks

IQVIA; Melbourne; Hybrid; AUD 105,000 - 125,000; Full time

Benefits offered by this job

Car allowance

Health allowance

Hybrid work environment

Job summary

IQVIA is seeking a Clinical Research Associate for roles across Australia. You will monitor sites, manage protocol training, and ensure data quality in line with GCP/ICH and sponsor requirements.

You will build site relationships, track regulatory submissions and recruitment, and support start-up activities where applicable. The role offers a flexible hybrid model with competitive salary and benefits.

Qualifications

• Bachelor's Degree in scientific discipline or health care.
• Requires at least 9 months of independent on-site monitoring experience.
• GCP/ICH regulatory knowledge and company training.
• Strong organizational and communication skills.
• Proficiency with Microsoft Word, Excel and PowerPoint.

Responsibilities

• Perform site monitoring visits per GCP/ICH and scope of work.
• Coordinate recruitment and manage project expectations with sites.
• Administer protocol training and maintain regular site communications.
• Track submissions, enrollments, CRFs and data queries.
• Maintain Trial Master File and Investigator Site File documentation.

Skills

Site monitoring

GCP/ICH knowledge

Regulatory knowledge

Project coordination

MS Word / Excel / PowerPoint

Education

Bachelor's Degree in scientific discipline or health care

Tools

MS Word

Excel

PowerPoint

Mobile devices (iPhone / iPad) usage

Job description

IQVIA is seeking a Clinical Research Associate for roles across Australia. You will monitor sites, manage protocol training, and ensure data quality in line with GCP/ICH and sponsor requirements.

You will build site relationships, track regulatory submissions and recruitment, and support start-up activities where applicable. The role offers a flexible hybrid model with competitive salary and benefits.