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Covance Lithuania is looking for Clinical Research Associates! (office - Oferta z Jobs.pl

Administracja biurowa » Pracownik biurowy

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  • AdresLithuania,
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Covance Lithuania is looking for Clinical Research Associates! (office

Nr ref.: /JOBS.pl

  • At the moment we are looking for:

    Clinical Research Associates on different levels - CRA I, CRA II and Senior CRAs in Lithuania (office or home based) - this is a great moment to join us ! - up to EUR 5000 Sign on Bonus!

    As CRA you will be responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits.


    Site administrating and site monitoring responsibility for clinical studies according to Standard Operating Procedures, ICH Guidelines and GCP;
    Recruiting potential investigators, preparing EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor;
    Completing Serious Adverse Event (SAE) reporting, processing production of reports;
    Negotiating study budgets with potential investigators and assisting the legal department with statements of agreements as assigned;
    Interact with internal work groups to evaluate needs, resources and timelines;
    Assist with training, mentoring, and development of junior employees, e.g. co-monitoring (for CRAs II);
    Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned (for CRAs II).
    Required skills, experience and education:
    Minimum 1 year of relevant clinical research experience in pharmaceutical or CRO industries;
    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 English language.
    Understanding of the clinical trial process;
    Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements;
    Thorough knowledge of monitoring procedures.

    In return, we offer you the opportunity to develop your career with an international organization; to pursue further training and to take advantage of our flexible conditions and attractive remuneration package.

    Your rewards :
    ° Up to a EUR 5,000 sign on bonus - limited time only, apply now!
    ° The opportunity to pursue further training and an interesting career in an inspiring environment that values achievement, supports a balance between your personal and professional life and allows you to make meaningful contributions
    ° Flexible conditions and an attractive remuneration package


    Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.


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