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CRA II - Oncology - Russian Federation - Oferta z Jobs.pl

Administracja biurowa » Pracownik biurowy

  • Województwozagranica
  • Miejscowośćinne
  • AdresRussian Federation,
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CRA II - Oncology - Russian Federation

Nr ref.: /JOBS.pl

  • From our early days as an academic CNS research organization in the 1980s, to the formation of INC in 1998, to where we are today, we've continued to improve what we do.

    We understand that cancer is not one disease, but a category of widely varying diseases, each with its own specialized scientific complexities, patient populations and range of treatment options. Our Oncology and Hematology practice is dedicated to the execution of clinical trials in these complex indications and is staffed by dedicated professionals with backgrounds in oncology drug development in academia, industry and CRO settings. This expertise, combined with INC Research's Trusted Process® methodology for delivering dependable trial outcomes, provides the resources, clinical expertise and development know-how to help our clients with every facet of their Oncology research

    We are currently looking to strengthen our Clinical Monitoring team in Russia and are seeking a CRA for our Oncology Department to be based in either our Moscow or St.Petersburg office. We can also accept home office based workers too.


    Core responsibilities:
    A brief summary of duties you will be involved in:

    • Monitoring all types of clinical trials and participating in all types of site visits ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
    • Data Handling, Reporting, Tracking and administrative tasks
    • Performing management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines.

    Skills and attributes:
    To succeed in this role you will need the following skills/experience:

    • Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position
    • Previous nominal practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO
    • Basic understanding of SOPs, WIs, FDA, and local regulations as well as ICH GCP guidelines
    • Good command of written and spoken English language

    Why choose us:
    It takes skill and passion to develop medicines the way we do. Don't worry - if you've got the passion part, we'll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.
    We've got an attitude at INC: "Can do, I own it." Absolutely everyone has ownership of what they do here. And because we're given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.
    "We were ranked "Top CRO" to work with in the CenterWatch 2013 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide)."

    What happens next:
    If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.


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