IQVIA is seeking an experienced Clinical Research Nurse to support a clinical research site in Concord, Sydney. This part-time role offers the chance to contribute to high-quality clinical trials within a team-oriented research environment.

Key Responsibilities
Support patient screening, recruitment, and enrollment, including informed consent and pre-consent activities
Collect medical and concomitant medication history
Perform and document vital signs (including height and weight) and ECGs
Provide administrative support for AE/SAE documentation and reporting per protocol and regulatory requirements
Manage Investigational Product (IP): receipt, storage, accountability, preparation, dispensing, administration, and return/destruction
Collect, process, and ship laboratory samples
Enter, verify, and correct source data in CRFs, EDC, eCOA, and other study systems; manage data queries
Maintain the Investigator Site File, including IRB/IEC submissions and communications
Use IVRS/IXRS and other trial-related systems




Coordinate patient scheduling and provide ongoing participant support
Support recruitment initiatives, referrals, and community/physician outreach
Perform general study-related administrative tasks, including EMR printing and certification

Required Qualifications & Experience
Nursing qualification with current RN registration
Minimum 3 years’ experience as a Research Nurse in clinical trials
Cardiovascular experience as an advantage or would be a plus
Solid knowledge of clinical trial conduct, protocols, consent processes, and medical terminology
Proven experience with IP handling, ECGs, vital signs, and laboratory procedures
Proficiency in MS Office and clinical trial systems (EDC, IVRS/IXRS)
Excellent communication, organizational skills, and attention to detail

Why IQVIA?

Join a global leader in clinical research and healthcare innovation. At IQVIA, you’ll work on impactful studies in a supportive and skilled environment.
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📌 Clinical Research Nurse Sydney (Australia)
🏢 Iqvia
📍 Australia