Trabajos

    Clinical Trial Administrator II - Buenos Aires, Argentina - PSI

    PSI
    PSI Buenos Aires, Argentina

    hace 4 días

    Default job background
    De jornada completa
    Descripción

    Job Description

    Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

    Hybrid position in Buenos Aires, Argentina

    Only CVs in English will be accepted.

    You will be responsible for:

  • Customization of Site ICF/patient documents before sending it to sites;
  • EC- IRB submissions;
  • Site Room, Veeva Vault, electronic Trial Master file and CTMs (including set up and maintenance);
  • Site file preparation for SIV (Printing and assembling documents);
  • Collection and filing documents from sites for MOH submissions;
  • Coordinate the translation of documents;
  • Collection/QC/filing of site documents– all documents required per Data Management Plan, not limited to Investigational Product Release-Enabling Document;
  • Accesses to systems: Collecting vendor access information from sites in the format requested.
  • #LI-Hybrid

    Qualifications

  • College/University degree or an equivalent combination of education, training & experience;
  • Minimum 1 year of industry experience
  • Administrative work experience, preferably in an international setting;
  • Local regulations knowledge
  • Prior experience in Clinical Research;
  • Full working proficiency in English and Spanish;
  • Proficiency in MS Office applications;
  • Ability to plan and work in a dynamic team environment;
  • Communication and collaboration skills.
  • Additional Information

    Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.



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