Clinical Trials Assistant

5 days ago

Sydney, Australia IQVIA Full time

As a Clinical Trials Assistant (CTA) you will support the clinical project team in the following areas: accurately update and maintain clinical systems within project timelines; prepare, handle, distribute, file, and archive clinical documentation and reports; review of study files periodically for accuracy and completeness; prepare, handle and distribute of Clinical Trial Supplies and maintenance of tracking information; track and manage Case Report Forms (CRFs), queries and clinical data flow. May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. Perform administrative tasks to support team members with clinical trial execution as needed.

**Qualifications**:

- Minimum 6-12 months experience in a CTA role.
- Experience accurately updating and maintaining clinical documents and systems (e.g., eTMF and CTMS).
- Exceptional communication, computer, and problem-solving skills.
- Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- High or Secondary School diploma/certificate or country’s educational equivalent and 3 years administrative support experience; or equivalent combination of education, training, and experience.

**Benefits**:

- Full flexibility to work from home or come to our brand-new offices in SYD/MEL
- Well-established onboarding and continuous training and development opportunities
- IQVIA benefits including extra leave and health allowance
- Being part of a company that promotes and supports a healthy work life balance
- Strong, stable and experienced team and supportive managers
- Parental leave Fantastic inclusive IQVIAN work culture

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