Clinical Research Administrator Assistant

1 semana atrás


Lisboa, Lisboa, Portugal Iqvia Argentina Tempo inteiro

Job Overview


Iqvia Argentina is seeking a Clinical Trial Assistant/Start-Up to perform daily administrative activities, ensuring a complete and accurate Trial Master File delivery. This role assists in the coordination and administration of study activities from start-up to execution and close-out, within the Local Study Team (LST), guaranteeing quality and consistency of study deliverables to time, cost, and quality objectives.



About the Role

This position requires assisting Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams with accurately updating and maintaining clinical documents and systems like Trial Master File that track site compliance and performance within project timelines.



  • Assist CRAs and RSU with preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • 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.
  • Maintenance of regulatory files and adherence to Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

The ideal candidate will possess high school or university diploma qualifications, preferably with experience in clinical research administrative support. Strong computer skills, including Microsoft Word, Excel, and PowerPoint, are required. Excellent written and verbal communication skills, including proficiency in English language, are necessary. Additionally, effective time management and organizational skills, as well as basic knowledge of applicable clinical research regulatory requirements, are essential for success in this role.



Requirements

  • 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
  • Basics knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Knowledge of applicable protocol requirements

Salary: $50,000-$65,000 per year.



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