Clinical Resarch Nurse - Concord NSW
On-siteNorth Sydney, New South Wales, Australia
Job Summary
Support patient screening, recruitment, and enrollment, including informed consent and pre-consent activities. Collect medical history, perform vital signs, ECGs, and laboratory sample collection. Manage Investigational Product from receipt to return and document AEs/SAEs per protocol. Enter and verify source data in CRFs, EDC, and eCOA systems while maintaining the Investigator Site File. Coordinate patient scheduling and provide ongoing participant support through community and physician outreach. This part-time role (16 hours/week) is based in Concord, NSW, with a start date of ASAP and a duration of approximately six months. Join IQVIA to contribute to high-quality clinical trials within a collaborative research environment.
Required Qualifications
- Nursing qualification with current RN registration
- Minimum 3 years' experience as a Research Nurse in clinical trials
- 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
Desired Qualifications
- Cardiovascular experience as an advantage or would be a plus
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