Clinical Research Coordinator in Macquarie Park
Working Hours:
24 hours per week, some shift work and Saturday work might be required
Start Date
: Immediately
Duration
: Approximately 8 months
IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Macquarie Park .This
24h hour per week
role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Key Responsibilities
As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:
Prescreening and Screening tasks
Review charts from the site data base
Maintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and eTMFs
Supporting patient screening and enrollment, including handling informed consent and privacy documentation
IP - site accountability including IP - patient compliance
Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations
Processing and shipment of lab samples process
Printing and certifying EMR
Coordinating logistical activities for study procedures in line with the study protocol




Communicating with study monitors and responding to study-related inquiries
Carrying out general administrative tasks related to the study
Your Profile
We are looking for candidates who bring a combination of education, experience, and skills:
Bachelor's degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
Experience with lap samples and IRT/IWRS systems
Good knowledge of medical terminology
Robust IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
Excellent interpersonal and communication skills
Strong organizational skills and attention to detail
Why Join IQVIA?
At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.
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📌 Clinical Research Coordinator (Sydney)
🏢 IQVIA
📍 Sydney