Clinical Research Nurse - Concord NSW

IQVIA Inc; Sydney; Hybride; AUD 55 000 - 96 000; Temps partiel

Résumé du poste

IQVIA seeks an experienced Clinical Research Nurse to support a Concord, NSW site. This part-time role (16 hours/week) starts ASAP for ~6 months, with exposure to high-quality clinical trials in a collaborative environment.

You will screen and enroll patients, perform vital signs and ECGs, handle IPs, collect lab samples, and enter data in CRFs/EDC; apply regulatory standards and coordinate scheduling with participants.

Qualifications

• Nursing qualification with current RN registration.
• Minimum 3 years’ experience as a Research Nurse in clinical trials.
• Cardiovascular experience is advantageous.
• Proficiency in MS Office and clinical trial systems (EDC, IVRS/IXRS).
• Excellent communication and organizational skills.

Responsabilités

• Support patient screening, recruitment, and enrollment with informed consent.
• Perform and document vital signs, ECGs, and collect samples.
• Manage IP receipt, storage, dispensing, and destruction.
• Enter and verify data in CRFs, EDC, and other systems; handle queries.
• Maintain Investigator Site File, handle regulatory submissions.
• Coordinate scheduling and provide participant support.
• Perform general study-related admin tasks.

Connaissances

RN registration

Clinical trial experience

ECGs

Communication skills

Data entry (CRFs/EDC)

Formation

Nursing qualification with RN registration

Outils

EDC

IVRS/IXRS

MS Office

Description du poste

Clinical Research Nurse - Concord NSW### Clinical Research Nurse - Concord NSWApply: North Sydney, New South Wales, Australia: Part time: Posted Today: R1577070# Clinical Research Nurse**Location:** Concord NSW **Work Type:** Part-time (16 hours/week) **Start Date:** ASAP **Duration:** ~6 monthsIQVIA 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-OnsiteIQVIA 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.comIQVIA 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.