PRAHS

  • Drug Supplies Coordinator - Business Process Analyst

    Job Locations - | US-PA | US-PA
    Posted Date 6 days ago(4/20/2018 11:45 AM)
    ID
    2018-45768
  • Overview

    Do you want to be responsible for developing drug supply planning strategy and overall management of supplies for clinical studies.

     

     

    Who are we?

    We Are PRA.

     

    We are 15,000+ employees strong, operating in more than 85 countries. We are committed to saving lives, and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We are getting live saving drugs into the hands those who need them most.

     

    Who Are You?

     

    You are an experience professional with a passion for clinical supplies. You are organized, but flexible and adaptable to unexpected changes. You can easily envision the bigger picture, without losing sight of the day-to-day tasks. You can provide excellent leadership to not only your project teams, but also to clients. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.

     

    Still here? Good. Because if this is you, we’d really like to meet you.

     

    Responsibilities

    What will you be doing?

     

    You will be working in partnership with the scientific, business, operational, clinical and technology areas to support the execution of global clinical trials in the area of global clinical supply management.

     

    What do you need to have?

    • Provide support as global clinical supplies Business Process Analyst
    • Engage with the GCS community to develop and implement new processes and to assess and modify existing processes where needed.
    • Support the implementation and execution of integrated Business Process Management, enabling coordinated and timely execution of GCS business changes and improvements.
    • Respond to questions and/or concerns from external stakeholders, including Global Clinical Trial Organization and Global Development Quality, about the execution of GCS processes and procedures
    • Support GCS responsibilities related to Veeva Vault Trial Master File, including GCP inspection preparation activities.
    • Provide support as a Process Modeler using Casewise and NIMBUS process mapping tools

    Qualifications

    • Minimum of 2 years relevant work experience. 
    • A Bachelor’s degree in health sciences or related field preferred.
    • 2 – 4 years of prior experience in a pharmaceutical, biotech and clinical supply logistics environment preferred
    • SAP experince preferred.

     

    To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.


    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with di



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