Hiring.Camp

Clinical Research Nurse - Concord NSW

Iqvia

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Location
Melbourne, Australia
Workplace
Onsite
Type
Part-time
Department
Healthcare
Experience
3+ years
Source
Workday

Description

Clinical Research Nurse

Location: Concord NSW
Work Type: Part-time (16 hours/week)
Start Date: ASAP
Duration: ~6 months

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.

Interested?
Apply today to be part of meaningful clinical research with IQVIA.

#LI-HCPN

#LI-CES

#LI-DNP

#LI-NS1

#LI-Onsite

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Skills

EMRClinical Trials

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