Clinical Research Coordinator
hace 1 mes
Clinical Trial Administrator
Job Overview:
Clinical Trial Administrators perform daily administrative activities to ensure a complete and accurate Trial Master File delivery. They assist in the coordination and administration of study activities from start-up to execution and close-out, ensuring quality and consistency of study deliverables to time, cost, and quality objectives.
Key Responsibilities:
- Assist Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems.
- Prepare, handle, distribute, file, and archive clinical documentation and reports according to standard operating procedures.
- Review study files for completeness and assist with periodic reviews.
- Coordinate the tracking and management of Case Report Forms, queries, and clinical data flow.
- Act as a central contact for clinical team communications, correspondence, and associated documentation.
Requirements:
- High School or University Diploma
- Clinical research administrative support experience preferred
- Computer skills, including Microsoft Word, Excel, and PowerPoint
- Written and verbal communication skills, including good command of Spanish and English language
- Effective time management and organizational skills
- Ability to establish and maintain effective working relationships
- Basic knowledge of applicable clinical research regulatory requirements
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.
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