Clinical Research Nurse - Concord NSW

About the role

IQVIA is seeking an experienced Clinical Research Nurse to support a clinical research site in Concord, Sydney. This is a part-time role of about 16 hours per week, starting as soon as possible and lasting around 6 months, in a collaborative research environment.

Key responsibilities

• Support patient screening, recruitment and enrolment, 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 the investigational product: 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, and 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 profile

• Nursing qualification with current RN registration
• Minimum 3 years' experience as a Research Nurse in clinical trials
• Cardiovascular experience is an advantage
• Strong knowledge of clinical trial conduct, protocols, consent processes and medical terminology
• Proven experience with IP handling, ECGs, vital signs and laboratory procedures
• Excellent communication, organisational skills and attention to detail

Required skills

• Proficiency in MS Office
• Proficiency in clinical trial systems (EDC, IVRS/IXRS)