Join 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 Aires

You will:

- Be the point of contact for clinical project teams, support services and client companies on safety reporting matters
- Coordinate accurate and time-bound reporting of safety issues to authorities
- Be responsible for document management, such as filing, processing, and quality control
- Update and maintain tracking systems, knowledge repositories, working files, and schedules

- College/University degree or an equivalent combination of education, training & experience
- Life Sciences degree is a plus
- Prior experience in Clinical Research required, with focus on regulatory aspects of safety reporting
- Full working proficiency in English
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment with tough deadlines
- Communication and collaboration skills

Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.

📌 Regulatory Officer (Buenos Aires)
🏢 Psicro
📍 Buenos Aires