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    “Great companies are built on great leaders,
    outstanding companies are built on outstanding people”
    J. Spaas

    Our company

    Global Stem cell Technology (GST) NV is a veterinary biotech company which was founded in 2012 to develop and produce state-of-the art stem cell products for horses and dogs. The research and development department of the company performs scientifically superior studies in order to create robust, reproducible and reliable products. The production and quality department are responsible for the validation of the new products and techniques and for high-scale production of these advanced stem cell products under GMP circumstances. 

    Subsequently, the clinical trials unit investigates the safety and efficacy of these products from clinical phase I up to clinical phase III. GST thus translates regenerative medicine into evidence-based clinical applications. Thanks to the highly efficient interdepartmental collaboration, the company is known for robust and reliable product development where integrity, high quality services, and animal welfare are solid company values. The young driven, divers and dynamic team and the horizontal hierarchical structure assemble the foundation of the friendly and familiar atmosphere present.

    Clinical Research Associate

    Nauwgezette collega die actief wil meedenken

    Function

    • As a CRA, you are responsible for the site monitoring for clinical trials according to our Standard Operating Procedures and GCP guidelines.
    • You develop and write the trial protocols (outlining purpose and methodology) and you design the data collection forms. You make sure that the right materials and documents are available, and you communicate with the ethics committee.
    • You monitor the clinical trial throughout its duration, which involves visiting the trial site on a daily basis. Afterwards, you write visit reports and you prepare the final report.
    • You also have regulatory affairs responsibilities such as preparation of submissions for lifecycle management for approved products, investigational products and new product applications. This also includes the coordination of global submissions to various regulatory agencies and external partners.
    • Your office and the clinical trial site are located in Evergem. You end up in a small team and you report to the Head of clinical trials.

    Profile

    • You have a University degree in Veterinary Sciences, preferably specialized in pet animals. A FELASA C certificate is an asset.
    • You are detail-oriented and you understand the importance of administration.
    • You speak and write English as a native. Knowledge of Dutch is an advantage, because all your colleagues are Dutch speaking
    • You work independently but you have the social skills to work in a small team as well
    • Experience in Regulatory Life Cycle Management and eCTD is an advantage, although not required.

    We offer you

    We offer you the chance to be part of a stable laboratory group. In our organization, everyone is accessible. We support our employees in realizing their personal growth, we invest in their talents and ambitions, and we offer interesting trainings and challenging projects.

    We offer our employees a competitive salary package (including group and hospitalization insurance, meal vouchers,…), a daily bowl of soup and fresh fruit. We also take the lead in organizing numerous activities after working hours.

    Interested?

    Your application will be considered quickly and with the greatest confidentiality. For additional information please contact Annelies De Vos: jobs@anacura.com or by phone +32 9 257 15 07.

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