Job DescriptionJoin our international team and support regulatory safety reporting aspects of clinical research projects, streamlining communication, maintaining electronic systems and managing documents.Office-Based in Buenos AiresYou will:Be the point of contact for clinical project teams, support services and client companies on safety reporting mattersCoordinate accurate and time-bound reporting of safety issues to authoritiesBe responsible for document management, such as filing, processing, and quality control Update and maintain tracking systems, knowledge repositories, working files, and schedulesQualificationsCollege/University degree or an equivalent combination of education, training & experienceLife Sciences degree is a plusPrior experience in Clinical Research required,



with focus on regulatory aspects of safety reportingFull working proficiency in EnglishProficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environment with tough deadlinesCommunication and collaboration skillsAdditional InformationAdvance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.Please let us know if any additional information is needed at this point.
And as agreed, would be great fi you set up a Teams chat for Natalia and me, so that we could promptly see your messages and react to them.

📌 Regulatory Officer (Safety Reporting) (Buenos Aires)
🏢 Psi Cro
📍 Buenos Aires