Clinical Trial Administrator.

Job DescriptionJoin our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. 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-HybridQualificationsCollege/University degree or an equivalent combination of education, training & experience;Administrative work experience, preferably in an international setting;Local regulations knowledgePrior 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 InformationAdvance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.