Document Specialist

Job Description If you are keen to provide administrative, document management support to pharmaceutical research projects, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you! Only CVs in English will be considered. Responsibilities for this role include:  Maintaining PSI and client Trial Master File (TMF), as applicable Archiving document hard copies in a standardized way Reviewing and reporting TMF completeness to project teams, as applicable  Ensuring compliance with applicable procedures and policies Qualifications Bachelor's degree;  Prior administrative experience Experience in archiving is a plus Full working proficiency in English and Spanish; Portuguese is a plus   Proficiency in standard MS Office applications Detail-oriented mindset and ability to do paperwork Good organizational and time-management skills Additional Information All your information will be kept confidential according to EEO guidelines.