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