PRAHS

  • Regional Clinical Studies Associate (Home-Based)

    Job Locations (All) | US-Remote
    Posted Date 3 weeks ago(10/22/2018 2:02 PM)
    ID
    2018-49845
  • Overview

    As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

     

    At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

     

    At PRA, borders do not create boundaries.  PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals.  Our growing workforce is comprised of over 15,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community.

    Responsibilities

    Develops/maintains study documents and utilizes company systems to manage clinical biomedical studies.  Provides administrative support to project team members in clinical operations and project management.   Works with the project team to ensure that projects are completed in accordance with contract and client expectations.  Completes project management tasks as assigned by the study project manager/project director.  Project management tasks will provide opportunities to broaden exposure to project management activities and to develop core project management skills. 

     

    • Expert knowledge of applicable systems/processes
    • Proficiency in using applicable business applications including word processing, spreadsheet, presentation programs
    • Basic knowledge of basic principles of timeline management, project financials, and risk management
    • Working knowledge of the company’s industry and service offerings
    • Understanding of relevant regulations
    • Familiarity with medical terminology
    • Read, write and speak fluent English; fluent in host country language
    • Advanced knowledge of some functional activities based on previous work assignments
    • Understanding of client contract, scope of work

    Qualifications

     

    REQUIRED EXPERIENCE:

    • 3 years’ experience in clinical research in a similar position 
    • Bachelor’s degree or international equivalent in business, finance, health sciences, or related field  
    • Experience with Study Start-up, regulatory documentation collection and quality control

     

    PREFERRED EXPERIENCE:

    • Experience working with Investigator Initiated Studies - Highly preferred
    • Experience working within clinical systems, electronic trial master file - 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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