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. **Job Description**: 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-Remote_ **Qualifications**: - College/University degree or an equivalent combination of education, training & experience; - Administrative work experience, preferably in an international setting; - Local regulations knowledge; - Prior experience in Clinical Research; - Full working proficiency in English and Spanish; - 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.