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  • Posted: Nov 14, 2019
    Deadline: Not specified
  • The story of PRA Health Sciences would naturally talk about how we’ve become one of the world’s largest CROs. It would talk about our innovation and growth and would speak to our operational efficiencies and transparency. It would highlight our expertise and customization. And it would touch on the incredible differences we’ve made, over ou...
    Read more about this company

    Regulatory and Start-up Manager

    As a Regulatory and Start-up Manager you will be dedicated to one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, Alzheimer’s and infectious diseases. Be ready to work in a solid partnership and an environment driven by innovation and continuous improvement.

    The Regulatory and Start up Manager is accountable for execution and oversight of local operational clinical trial activities in a country for assigned protocols in compliance with ICH/GCP and country regulations, policies and procedures, quality standards and adverse event reporting requirements internally and externally.


    • Ownership of country and site budgets
    • Development, negotiation and completion of Clinical Trial Research Agreements
    • Responsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols
    • Responsible for managing country deliverables, timelines and results for assigned protocols to meet country commitments
    • Responsible for quality and compliance in assigned protocols in the country
    • Oversight and coordination of local processes
    • Responsible for clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process

    You are:

    Passionate, innovative and committed.

    Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

    • A minimum of a Bachelor’s degree in Life Sciences
    • 5 years prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment
    • Solid experience in start up activities
    • A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essentia
    • Fluent Afrikaans and English language is a must

    Method of Application

    Interested and qualified? Go to PRA Health Sciences on to apply
  • Send your application

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