Job Properties
  • Job Type
    Full-time Position
  • Category
    Cleaning & Landscaping
  • Languages
  • Experience Required
  • Degree Required
    • Province
    • Date Posted
      August 10,2022
    • IMG_6430
    • VISA
    • Premium Package

    Clinical Trail Assistant

    Job profile
    Job mission
    In the final phase of Synthon’s drug development program for generic medicines, the Clinical Research & Development and Toxicology department conducts clinical trials to demonstrate bioavailability and bioequivalence of our medicines.
    As a Clinical Trial Assistant you will be working on bioavailability and bioequivalence trials initiated by Synthon and provide support to the Clinical Trial Teams.
    You are involved in the many different logistical and operational activities in conjunction with the set-up and execution of the clinical trials including contracting, vendor management, insurance, financial overviews, filing and archiving.
    You assist in the preparation of different types of documents that are being used in the preparation and execution of clinical trials.
    You are involved in maintaining the Clinical R&D Quality Management System.
    You also assist in the planning, organization and execution of meetings, such as Clinical Trial Team meetings, R&D events, and/or Investigator meetings.
    It is expected that you quickly work independently on multiple projects in parallel and have an intuitive feel for optimal organization and logistics for your projects.
    You enjoy working in a fast-paced organization. You work within a team of approximately 10 Clinical Research & Development professionals and will report to the vice president Clinical Research & Development and Toxicology. Your profile
    Your profile
    Your letter of motivation and CV should show that you have:
    a bachelor or master’s degree in life sciences or other relevant education.
    a good command of the English language, both in writing and speaking
    excellent attention to detail and initiative.
    able to work within a team, liaising efficiently with internal departments and third parties.
    ability to manage a high workload and the pressure of deadlines.
    Personal skills
    You have excellent planning and organizational skills and an eye for detail. You are a good communicator: you are able to clearly explain to internal and external parties what needs to be done and what you expect. You are expected to keep all parties involved well-informed and updated. Your approach to work is pragmatic and structured, but you are also open-minded and flexible when required. Application
    Our offer
    We offer our employees:

    • A professional, yet pleasant and informal working environment with short communication lines, focus on cooperation and appreciation of initiatives
    • Competitive remuneration
    • Good working conditions
    • A keen eye on work/life balance
    • Inspiring company events.

    Application and important dates
    If you are interested in this position, we look forward to your application. You can apply via our website Please send your application (English motivation letter and resume) before 8 September 2022. The first round of interviews will take place 15 September 2022 and consists of more round of interviews.
    For further information, please contact Sandra van Os (vice president Clinical R&D and Toxicology), at tel. +31(0)24 3727700.

    Job Type: Full-time

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