
Clinical Administrator
5 days ago
Clinical Project Coordinator
You will provide administrative support to clinical projects, ensuring timely and accurate completion of tasks. This role offers a hybrid working arrangement with two days of flexible work from our North Ryde office.
Key Responsibilities:- Prepare, handle, and distribute Clinical Trial Supplies, maintaining tracking information.
- Update and maintain clinical documents and systems (e.g., eTMF and CTMS) for site compliance and performance within project timelines.
- Serve as a central point of contact for designated project communications, correspondence, and associated documentation.
- Accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and approval.
- Minimum 6-12 months experience in a CTA or similar role.
- Awareness of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Exceptional communication, computer, and problem-solving skills.
- High school diploma/certificate or equivalent, and three years of administrative support experience; or an equivalent combination of education, training, and experience.
- Ongoing training and development opportunities.
- IQVIA benefits, including extra leave and health allowance.
- A supportive team environment and healthy work-life balance.
- Parental leave and an inclusive work culture.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We create intelligent connections to accelerate the medical treatment development and commercialization process, improving patient outcomes worldwide.
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