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  • Posted: Aug 16, 2021
    Deadline: Not specified
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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...
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    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

    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.

    Method of Application

    Interested and qualified? Go to PSI CRO AG on jobs.smartrecruiters.com to apply

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

  • Send your application

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