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Senior Clinical Research Associate - Oncology - Germany - Oferta z Jobs.pl

Administracja biurowa » Pracownik biurowy

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Senior Clinical Research Associate - Oncology - Germany

Nr ref.: /JOBS.pl

  • We are currently looking to strengthen our Clinical Monitoring team in Germany and are seeking a Senior CRA for our Oncology Department to be based in either our Munich or Langenfeld office. We can also consider home 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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