Clinical Trial Administrator Ii

3 semanas atrás


São Paulo, Brasil Psi Cro Tempo inteiro

Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Join 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-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 Portuguese 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. #J-18808-Ljbffr


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