Clinical Resarch Nurse - Concord NSW at IQVIA. - Turkey

Sydney, New South Wales, Australia -

Full Time

Start Date

Immediate

Expiry Date

16 Jun, 26

Salary

0.0

Posted On

18 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Patient Screening, Recruitment, Informed Consent, Vital Signs, ECGs, AE/SAE Documentation, Investigational Product Handling, Laboratory Sample Processing, Source Data Entry, EDC Systems, Investigator Site File Management, IVRS/IXRS, Patient Scheduling, Clinical Trial Conduct, RN Registration, Cardiovascular Experience

Industry

Hospitals and Health Care

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. 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.

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Responsibilities

Key responsibilities include supporting patient screening, recruitment, enrollment, managing vital signs and ECGs, and handling administrative documentation for adverse events. The role also involves managing Investigational Product, processing lab samples, and accurately entering source data into various study systems.