• Site Management Associate - 1

    Job Locations (All) | US-PA-Blue Bell
    Posted Date 2 weeks ago(10/30/2018 4:04 PM)
  • Overview

    Who are we?

    We Are PRA.


    We are 16,000+ 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 help get life-saving drugs into the hands of those who need them most.


    Who are you?


    You are someone who wants to be part of a fabulous group; a group that really supports their folks and promotes from within!  Science, Clinical Trials and Data are your passion, and you want to be a part of drug research and development, then this is for you!  You also enjoy tracking clinical studies and being a part of the big picture!


    Still here? Good. Because if this is you, Late Phase Services would love to meet you!




    What will you be doing?


    As a Site Management Associate, you will perform investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, in-house site management, and data review activities in accordance with the study protocol, client and/or PRA standard operating procedures (SOPs), and all applicable guidelines and regulatory requirements (e.g. ICH-GCP, and country/region specific).



    What do you need to have?



    • Read, write, and speak fluent English; fluent in host country language required.
    • Prior experience using computerized information systems required.
    • Extremely organized and don’t mind beingon the phone 90% of the time
    • Minimum of one year Clinical trials support, Data Coordination or pharmaceutical industry experience required.
    • Office-based or clinical experience required
    • Undergraduate degree or its international equivalent from an accredited institution is required.
    • A degree in a clinical, science, or health-related field is preferred.
    • Prior customer service experience preferred
    • Proficiency in additional languages preferred
    • Prior experience using computerized information systems required; experience with Electronic Data Capture, PC Windows, word processing, and electronic spreadsheets preferred
    • Knowledge of ICH and local regulatory authority drug research and development regulations 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 disabilities


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