Clinical Trials Assistant 1 - Sydney, Australia - IQVIA
Description
Job Overview:
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.
- 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 612 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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