Regulatory Officer

PSI CRO

1d • Onsite

About The Position

Join the international team and support regulatory safety reporting aspects of clinical research projects. The role focuses on streamlining communication, maintaining electronic systems, and managing documents. It is office-based in São Paulo.

Requirements

• College or university degree, or an equivalent combination of education, training, and experience.
• Prior experience in clinical research, with a 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.

Nice To Haves

• A degree in Life Sciences.

Responsibilities

• Serve as 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.
• Manage documents, including filing, processing, and quality control.
• Update and maintain tracking systems, knowledge repositories, working files, and schedules.

What This Job Offers

• Job Type: Full-time