Clinical Research Nurse - Concord NSW

QPL IQVIA RDS Poland Sp. z o.o.; Melbourne; On-site; AUD 55,000 - 83,000; Part time

Job summary

IQVIA Inc. seeks a qualified Clinical Research Nurse to join a Concord, NSW clinical site on a part-time basis (16 hours per week). The role supports patient screening, IP handling, data entry, and regulatory submissions in a high-quality trial environment.

Candidate must have an RN registration and at least 3 years in clinical trials, with ECGs, vital signs and lab procedures experience. Strong communication and organizational skills are essential.

Qualifications

• RN registration and nursing qualification.
• Minimum 3 years’ experience as a Research Nurse in clinical trials.
• Experience with IP handling, ECGs, vital signs, and lab procedures.
• Strong knowledge of clinical trial conduct, protocols and consent processes.
• Proficiency with MS Office and trial systems (EDC, IVRS/IXRS).
• Excellent communication, organization and attention to detail.

Responsibilities

• Screen patients and support recruitment, including consent.
• Collect medical history and vital signs; perform ECGs.
• Manage Investigational Product (IP) receipt, storage, dispensing and destruction.
• Collect, process and ship laboratory samples.
• Enter and verify data in study systems; handle data queries.

Skills

RN registration

Clinical trial experience

IP handling

ECGs

Vital signs

MS Office

EDC/IVRS/IXRS

Education

Registered Nurse (RN)

Tools

MS Office

EDC

IVRS/IXRS

Job 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.

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.

#LI-HCPN #LI-CES #LI-DNP #LI-NS1 #LI-Onsite

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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.