Clinical Research Sponsor Dedicated Paris

il y a 3 semaines


RueilMalmaison, Île-de-France PAR Fortrea France SARL Temps plein

Key Responsibilities:

  • Trial and Site Administration: Oversee the management of clinical trials, ensuring seamless site administration and compliance with regulatory guidelines.
  • Document Management: Maintain accurate and up-to-date documentation, adhering to Good Documentation Practices.
  • Regulatory and Site Start-Up Responsibilities: Coordinate with regulatory bodies and ensure timely site start-ups, meeting global and regional clinical research guidelines.
  • Budgeting, Agreement, and Payments: Manage budgets, negotiate agreements, and facilitate payments, ensuring financial transparency and compliance.
  • Meeting Planning: Organize and coordinate meetings, ensuring effective communication and collaboration among stakeholders.

    CORE Competency Expectations:

    • Language Proficiency: Fluency in local languages and business proficiency in English, with excellent verbal and written communication skills.
    • Global Clinical Research Knowledge: Good understanding of global, country/ regional clinical research guidelines and ability to work within these guidelines.
    • Good Documentation Practices: Hands-on knowledge of Good Documentation Practices.
    • IT Skills: Good IT skills, including MS Office and clinical IT applications, with the ability to adapt to new applications and strong MS Excel skills.
    • ICH-GCP Knowledge: ICH-GCP knowledge appropriate to the role.

    About Fortrea:

    Fortrea is a pioneering company revolutionizing the clinical trials development process. We are committed to delivering life-changing ideas and therapies to patients in need. Our collaborative workspace fosters personal growth, enabling you to make a meaningful global impact.



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