PRAHS

  • Study Manager - Oncology Early Development - Home Based

    Job Locations - | US-Remote | Canada-Remote
    Posted Date 2 days ago(7/20/2018 3:59 PM)
    ID
    2018-48064
  • Overview

    Do you want to watch clinical development change, or do you want to be the one to shape it?

     

    Because we’re hoping you’re here for the latter.

     

    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 lifesaving drugs into the hands those who need them most.

     

    Who are you?

    You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. 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.

    The Study Manager will be accountable for the operational planning, feasibility, and execution of a clinical protocol.

    Responsibilities

    What will you be doing?

    You will be accountable for being the supporting the operational execution of a clinical protocol. You will assist the Program Lead and protocol team with the conduct of clinical studies. You may have specific responsibilities for a single study or across multiple studies (e.g., data management deliverables, clinical supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). You may also be responsible for tracking study timelines and will be proficient in project management tools. You will share technical expertise with team members and you may interact with internal and external stakeholders (study sites, vendors, committees, etc) in support of clinical study objectives.

    Qualifications

    • A graduate degree or undergraduate degree.
    • Bachelor’s degree in the Life Sciences highly preferred
    • Study Manager level = 4+ years’; or MS with 3+ years’; or PhD with <2 years’ relevant career experience
    • Senior Study Manager level = 7+ years’; or MS with 5+ years’; or PhD with <2 years’ relevant career experience
    • Phase I Oncology experience and/or Phase I experience required
    • Pharmaceutical and/or clinical drug development experience.
    • Excellent oral (including presentation) and written communication, computer/database management and project management skills

    This is a home based position anywhere in the US or Canada

     

    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 disabilities.

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