Clinical Research Coordinator

hace 18 horas


Buenos Aires, Buenos Aires C.F., Argentina Iqvia A tiempo completo
Job Overview
A Clinical Trial Assistant provides administrative support to the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery. Key responsibilities include:
  • Assisting CRAs and RSU team with updating and maintaining clinical documents and systems.
  • Preparing, handling, distributing, filing, and archiving clinical documentation and reports according to standard operating procedures.
  • Maintaining site compliance and performance within project timelines.
The ideal candidate will have a life science degree, clinical research experience, and excellent communication skills.

Responsibilities

  • Track and manage Case Report Forms (CRFs), queries, and clinical data flow.
  • Prepare and handle Clinical Trial Supplies and maintain tracking information.
  • Act as a central contact for designated project communications and correspondence.
  • May accompany CRAs on site visits to assist with clinical monitoring duties.

Requirements

  • Life science degree or equivalent combination of education and experience.
  • Clinical research experience is highly valued.
  • Excellent computer skills including Microsoft Word, Excel, and PowerPoint.
  • Effective time management and organizational skills.
  • Awareness of applicable clinical research regulatory requirements.


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