• Study Start Up InHouse CRA-Wilmington NC

    Job Locations (All) | US-NC-Wilmington
    Posted Date 3 weeks ago(11/20/2018 4:34 PM)
  • Overview

    Do you want to use your skills and expertise to help change the world by playing a part in the development of new and innovative therapies?


    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 help get life-saving drugs into the hands of those who need them most.


    Who are you?


    You are flexible, efficient, proactive, and highly movitated.  You are able to  create and re-set priorities in a fast-paced environment without sacrificing your attention to detail.  You work well within a team, both in a leadership role and as a contributor.  You are a confident communicator, don’t take no for an answer, love a challenge, and can independently create solutions to complex issues. The idea of improving the lives of others by using your strategic and interpersonal skills excites you.  Despite a demanding day or difficult discussion, you are able to walk away with your positive attitude  intact.


    In your next career move, you want to work for a company that supports your professional growth and helps you find a work/life balance. You want to expand your knowledge, develop your skill set, and build your career.  Most of all, you want to do it in a place where you’re part of a team as zealous about their work as you are -- a place where you can really make a difference. 


    What will you be doing?

    You will be a key member of the Study Start-Up team. You will:

    • Interact successfully with both internal and external customers
    • Exhibit good decision making skills, utilizing all available resources for determing positive outcomes
    • Communicate with investigative sites and internal team members to predict timelines for site activation and ensure all activation requirements are met
    • Collect and review essential regulatory documents needed for site activation
    • Identify and escalate issues before they become critical
    • Adjust quickly to the changes of a dynamic organization
    • Update systems in a timely and accurate way
    • Be highly organized in an environment with shifting priorities
    • Analyze data and metrics relating to the site activation pathway
    • Learn and utilize various reporting tools


    What do you need to have?

    • 0 – 2 years of related experience
    • Undergraduate degree, health related preferred OR, an equivalent combination of education and experience sufficient to successfully perform the key responsibilities of the job
    • Flexibility with competing priorities
    • Exceptional time-management and communication skills
    • Familiarity with Microsoft Outlook, Word and Excel
    • Clinical trials support or pharmaceutical industry experience preferred
    • Knowledge of ICH and local regulatory authority drug research and development regulations preferred
    • Ability to read, write and speak fluent English required

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

    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.


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