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.

You will be asked to complete a short video screening as part of the interview process. We regret to inform you that we cannot consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.

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)

Communicated effectively with clients and stakeholders, mastered various computer applications, and resolved complex issues

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

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