Regulatory Affairs Assistant at PSI CRO AG

Job Description

Join our international team and support regulatory aspects of clinical research projects, streamlining communication, maintaining electronic systems and managing documents.

Office-Based in Pretoria, South Africa

You will:

• Be the point of contact for clinical project teams and support services on regulatory matters
• Prepare draft regulatory/ethics submission dossier
• Be responsible for document management such as filing, processing, translation, quality control 
• Update and maintain (automated) tracking systems, working files, and schedules
• Organize meetings, prepare agendas and minutes

Qualifications

• College/University degree or an equivalent combination of education, training & experience
• Life Science degree is a plus
• Administrative work experience, preferably in an international setting
• Prior experience in Clinical Research is a plus
• Full working proficiency in English
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication and collaboration skills

Additional Information

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