Clinical Trial Administrator Ii

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.