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CLINICAL RESEARCH ASSISTANT in Istanbul - Oferta z Jobs.pl

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  • Miejscowośćinne
  • AdresTurkey,
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  • COVANCE is probably enhancing your quality of life without you even knowing it. We play an important role in bringing new therapies to market by helping to turn raw compounds into safe, effective, and approved drugs that help people live longer, more productive lives.

    Our mission - bringing medical miracles to market sooner - impacts the lives of millions of people all over the world. Our current growth of Clinical Development Services (CDS) in Eastern European countries brings new opportunities not only for clinical roles, but also another business functions.

    CoSource, our insourcing division provides you with the opportunity to work directly for our clients. For these roles you will either work out of our client offices or field based - and see clinical trials from the clients' perspective. We work in partnership with global and smaller pharmaceutical companies and can support you in your career development.

    At the moment we are looking for: CLINICAL RESEARCH ASSISTANT in Istanbul, Turkey.
    This is a full time, temporary (6 months contract) position in a Team assigned to single Sponsor.

    As Clinical Research Assistant you will be responsible for EC/RA submissions and provide clinical support for projects according to Covance Standard Operating Procedures, ICH Guidelines and GCP, develop and maintain tracking systems for clinical projects and assist in field monitoring responsibilities as assigned by supervisor.


    Ethic Commitee / Regulatory Affairs submissions
    Performing documents review, query generation and resolution against established data review guidelines, under direct supervision of Covance or client data management systems;
    Assisting with generation and reconciliation of queries to investigative sites/clients to resolve problem data;
    Assisting with the management of study supplies and organize shipments;
    Creating, updating, tracking, and maintaining study-specific trial management files, tools, and systems;
    Assisting the local project team members with other administrative activities as required (e.g. payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators' meetings).

    Required education, skills and experience:

    University Degree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology);
    Fluency in local and good knowledge of English language.
    Experience with Ethic Commitee / Regulatory Affairs submissions (desired)
    Basic understanding of biology and biological processes;
    Exhibit general computer literacy;
    Good oral and written communication skills;
    Ability to set priorities and handle multiple tasks simultaneously;
    Work efficiently and effectively in a matrix environment;
    Good organizational and time management skills.

    We Offer:

    Covance's ongoing success offers team members unsurpassed growth and career development opportunities at an international organization; to pursue further training and to take advantage of our flexible conditions and attractive remuneration package
    There is no better time to join us!


    project associate, project assistant, clinical trial assistant, CTA, clinical trials, clinical study, clinical studies, pharma, pharmaceutical, trial assistant, clinical trial admin, clinical trial administrator, trial admin, trial administrator, CPA, EC/RA submissions, Ethic Commitee / Regulatory Affairs submissions, GCP, ICH, Istanbul, Turkey


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