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.
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.