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  • Posted: Aug 16, 2021
    Deadline: Not specified
  • 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...
    Read more about this company


    Regulatory Affairs Assistant

    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


    • 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.

    Method of Application

    Interested and qualified? Go to PSI CRO AG on to apply

    Note: Never pay for any training, certificate, assessment, or testing to the recruiter.

  • Send your application

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