Clinical Research Coordinator
2 semanas atrás
Clinical Trial Assistants play a crucial role in the success of clinical trials at Iqvia Argentina. As a key member of the clinical team, you will be responsible for ensuring the quality and consistency of study deliverables, while meeting time, cost, and quality objectives.
Key Responsibilities:- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems, such as the Trial Master File.
- Prepare, handle, distribute, file, and archive clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Coordinate the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
- High School or University Diploma
- Clinical research administrative support experience preferred
- Computer skills, including working knowledge of Microsoft Word, Excel, and PowerPoint
- Written and verbal communication skills, including good command of Portuguese and English language
- Effective time management and organizational skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Basic knowledge of applicable clinical research regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Join our team of dedicated professionals at Iqvia Argentina and contribute to the success of our clinical trials.
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