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 Strong 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 professional workplace.

📌 Clinical Research Nurse Sydney (Australia)
🏢 Iqvia
📍 Australia