Study Operations Coordinator
hace 1 semana
This role plays a vital part in the success of our clinical trials, supporting the coordination and administration of study activities from start-up to execution and close-out. As a Clinical Trial Assistant, you will work closely with the Clinical Research Associates and Regulatory and Start-Up teams to ensure timely and accurate delivery of the Trial Master File.
Key Responsibilities:- Assist in updating and maintaining clinical documents and systems, ensuring site compliance and performance within project timelines.
- Prepare, handle, distribute, file, and archive clinical documentation and reports according to standard operating procedures.
- Conduct periodic reviews of study files for completeness.
- Coordinate the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
- Serve as a central point of contact for clinical team communications, correspondence, and associated documentation.
- High school or university diploma required.
- Clinical research administrative support experience preferred.
- Proficiency in Microsoft Office, including Word, Excel, and PowerPoint.
- Strong written and verbal communication skills, with a good command of English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with colleagues, managers, and clients.
- Familiarity with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, as well as applicable protocol requirements.
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are dedicated to pushing the boundaries of human science and data science to create a healthier world.
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