Job DescriptionIf 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 applicableArchiving document hard copies in a standardized wayReviewing and reporting TMF completeness to project teams, as applicable Ensuring compliance with applicable procedures and policiesQualificationsBachelor's degree; Prior administrative experienceExperience in archiving is a plusFull working proficiency in English and SpanishProficiency in standard MS Office applicationsDetail-oriented mindset and ability to do paperworkGood organizational and time-management skillsAdditional InformationOur mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors.
Our recruitment process is easy and straightforward, and we'll be there with you every step of the way.

📌 Document Specialist (Buenos Aires)
🏢 Psi Cro
📍 Buenos Aires