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PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on 'on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments t...
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
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.
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