Join a dynamic team driving cutting-edge clinical trials
As a CRA, you'll be the key link between sponsors and trial sites—ensuring studies run smoothly, data is accurate, and compliance is top-notch.
As part of our Sponsor dedicated team you will join not 1 but 2 Globally Companies.
This role is Perth or Brisbane based.
Minimum of 18 months monitoring experience is required.
Key Responsibilities
Lead site visits (selection, initiation, monitoring, close-out) per GCP/ICH standards.
Drive subject recruitment and site engagement to meet study goals.
Deliver protocol training and maintain strong site communication.
Monitor site performance, elevate quality issues, and ensure regulatory compliance.
Track study progress: submissions, enrollment, CRFs, and data queries.
Maintain Trial Master File (TMF) and Investigator Site File (ISF).
Document findings and follow-ups with clear, timely reports.
Collaborate with cross-functional teams to support project execution.
Manage site budgets and invoicing (if applicable).
What You Bring
Bachelor's in science or healthcare (or equivalent experience).
2+ year of on-site monitoring experience.
Haematology and Oncology.
Strong grasp of GCP/ICH and clinical trial protocols.
Tech-savvy: MS Office, iPhone/iPad, and remote tools.
Excellent communication, organization, and problem-solving skills.
Ability to build strong relationships with sites and teams.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Learn more at
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