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Clinical Trial Assistant / Senior Clinical Trial Assistant - Oferta z Jobs.pl

Administracja biurowa » Specjalista ds. administracji

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Clinical Trial Assistant / Senior Clinical Trial Assistant

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  • Clinical Trial Assistant and Senior Clinical Trial Assistant Opportunities in Spain!
    Office-based in Madrid - Full Time and Permanent Contracts!

    ClinTec International is actively recruiting for clinical professionals to join our expanding global company. By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits. In the past 12 months, we have expanded into 17 new countries with offices opening across the globe. Apply now and become part of our international team.

    Job Description

    Due to a period of sustained expansion, a number of outstanding career opportunities have arisen within ClinTec International, a truly unique CRO, for talented Clinical Trial Assistants to join our experienced team in Madrid.

    Responsibilities of the Clinical Trials Assistant:

    Ensure administrative work of clinical trials: Create Investigator Files and other study information, booklets, worksheets, etc
    Ensure timely translation and validation process of study materials (e.g. patient diaries, instructions, IC)
    Provide investigators with all forms and lists to start the site evaluation and site validation (initiation and start of study information)
    Ensure timely ordering of study tools
    Preparation of ethical and regulatory submissions
    Ensure protocol initiation processes
    Organization and documentation of regular study meetings
    Organization and documentation of local investigators meetings
    Provide professional presentation of study materials for CRA and investigator trainings
    Archiving of processes, including electronic SORF and Trial Master File

    Essential Criteria:

    High School Degree or equivalent
    Previous experience in a similar role working within the pharmaceutical or CRO environment
    Good knowledge of the clinical trial process
    Fluency in Spanish (both written and spoken)
    Fluency in English (both written and spoken)
    Strong organisational and communication skills
    Willing and able to work office based in Madrid


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