Clinical Trial Assistant

1 week ago

Sydney, New South Wales, Australia Iqvia Full time

We are currently seeking Clinical Trials Assistant **(**CTA) to join our sponsor-dedicated team in a client facing role. As a vital part of our team, our **Clinical Trials Assistants** **(**CTA) perform daily administrative tasks to support to clinical projects and update clinical systems and databases. This role is a true hybrid position with two days office requirements with our client in North Ryde.

You will also perform general administrative tasks as needed. You will have excellent communication, computer, and problem-solving skills, and you will be resourceful, analytical, adaptable, and organised. You will be a natural at building rapport with peers and site staff.

When you join IQVIA AUSTRALIA in our sponsor-dedicated team, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.

With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

**Essential Functions**:

- Prepare, handle, distribute, file, and archive clinical documentation and reports as per the scope of work and standard operating procedures
- Review study files periodically for completeness and accuracy
- Support CRAs and RSU with the management of Clinical Trial Supplies and tracking information
- Track and manage CRFs, queries and clinical data flow efficiently and effectively.
- Communicate with the clinical team and provide relevant project information, correspondence and documentation

**Qualifications**:

- Minimum 6-12 months experience in a CTA role
- Flexible and adaptable to different levels of education, training and experience
- Updated and maintained clinical documents and systems accurately (e.g., eTMF and CTMS)
- Familiar with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and ensured compliance in all clinical trials
- Completed High or Secondary School diploma/certificate

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