IQVIA is seeking an entry-level Administrative Support role to assist the Clinical Research Associates (CRAs) and RSU team with maintaining trial master files and regulatory documentation. The role involves handling, filing, and archiving study documents and supporting timely project delivery.
Responsibilities include assisting with study file reviews, clinical supplies tracking, data flow, and acting as a central communications contact. Some on-site support may be required after training.
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Clinical Trials Documentation Specialist in Sydney employer: IQVIA
IQVIA is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for freelance translators passionate about life sciences. With opportunities for professional growth and the potential for permanent positions, you will be part of a global community dedicated to making a meaningful impact in healthcare. Join us and enjoy the flexibility of remote work while contributing to projects that truly matter.
