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Clinical Trails Assistant
2 weeks ago
- Assist with accurately updating and maintaining clinical documents and systems (e.g., eTMF and CTMS) that track site compliance and performance within project timelines.
- Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.
Qualifications:
- Minimum 612 months experience in a CTA role.
- Experience accurately updating and maintaining clinical documents and systems (e.g., eTMF and CTMS).
- Exceptional communication, computer, and problemsolving 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:
- Hybrid work options for SYD/MEL
- Wellestablished 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
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.
Learn more at-
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